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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1800591

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:99574331 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
G>A / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.260807 (69033/264690, TOPMED)
T=0.24638 (19388/78690, PAGE_STUDY)
T=0.18154 (5130/28258, 14KJPN) (+ 18 more)
T=0.18156 (3043/16760, 8.3KJPN)
T=0.15273 (2257/14778, ALFA)
T=0.2478 (1587/6404, 1000G_30x)
T=0.2498 (1251/5008, 1000G)
T=0.2435 (1091/4480, Estonian)
T=0.2711 (1045/3854, ALSPAC)
T=0.2540 (942/3708, TWINSUK)
T=0.1509 (441/2922, KOREAN)
T=0.1305 (239/1832, Korea1K)
T=0.231 (231/998, GoNL)
T=0.128 (101/792, PRJEB37584)
T=0.215 (129/600, NorthernSweden)
G=0.395 (94/238, SGDP_PRJ)
T=0.435 (94/216, Qatari)
T=0.123 (26/212, Vietnamese)
T=0.33 (13/40, GENOME_DK)
G=0.50 (7/14, Siberian)
T=0.50 (7/14, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
MTTP : Intron Variant
Publications
17 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 14778 G=0.84727 A=0.00000, T=0.15273
European Sub 11270 G=0.83505 A=0.00000, T=0.16495
African Sub 2280 G=0.8667 A=0.0000, T=0.1333
African Others Sub 68 G=0.90 A=0.00, T=0.10
African American Sub 2212 G=0.8657 A=0.0000, T=0.1343
Asian Sub 116 G=0.948 A=0.000, T=0.052
East Asian Sub 100 G=0.94 A=0.00, T=0.06
Other Asian Sub 16 G=1.00 A=0.00, T=0.00
Latin American 1 Sub 68 G=1.00 A=0.00, T=0.00
Latin American 2 Sub 408 G=1.000 A=0.000, T=0.000
South Asian Sub 48 G=0.94 A=0.00, T=0.06
Other Sub 588 G=0.855 A=0.000, T=0.145


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 G=0.739193 T=0.260807
The PAGE Study Global Study-wide 78690 G=0.75362 T=0.24638
The PAGE Study AfricanAmerican Sub 32512 G=0.72269 T=0.27731
The PAGE Study Mexican Sub 10810 G=0.82683 T=0.17317
The PAGE Study Asian Sub 8316 G=0.8399 T=0.1601
The PAGE Study PuertoRican Sub 7918 G=0.7038 T=0.2962
The PAGE Study NativeHawaiian Sub 4532 G=0.7743 T=0.2257
The PAGE Study Cuban Sub 4230 G=0.7021 T=0.2979
The PAGE Study Dominican Sub 3826 G=0.7060 T=0.2940
The PAGE Study CentralAmerican Sub 2450 G=0.8110 T=0.1890
The PAGE Study SouthAmerican Sub 1980 G=0.8232 T=0.1768
The PAGE Study NativeAmerican Sub 1260 G=0.7563 T=0.2437
The PAGE Study SouthAsian Sub 856 G=0.654 T=0.346
14KJPN JAPANESE Study-wide 28258 G=0.81846 T=0.18154
8.3KJPN JAPANESE Study-wide 16760 G=0.81844 T=0.18156
Allele Frequency Aggregator Total Global 14778 G=0.84727 A=0.00000, T=0.15273
Allele Frequency Aggregator European Sub 11270 G=0.83505 A=0.00000, T=0.16495
Allele Frequency Aggregator African Sub 2280 G=0.8667 A=0.0000, T=0.1333
Allele Frequency Aggregator Other Sub 588 G=0.855 A=0.000, T=0.145
Allele Frequency Aggregator Latin American 2 Sub 408 G=1.000 A=0.000, T=0.000
Allele Frequency Aggregator Asian Sub 116 G=0.948 A=0.000, T=0.052
Allele Frequency Aggregator Latin American 1 Sub 68 G=1.00 A=0.00, T=0.00
Allele Frequency Aggregator South Asian Sub 48 G=0.94 A=0.00, T=0.06
1000Genomes_30x Global Study-wide 6404 G=0.7522 T=0.2478
1000Genomes_30x African Sub 1786 G=0.7436 T=0.2564
1000Genomes_30x Europe Sub 1266 G=0.7346 T=0.2654
1000Genomes_30x South Asian Sub 1202 G=0.6173 T=0.3827
1000Genomes_30x East Asian Sub 1170 G=0.8624 T=0.1376
1000Genomes_30x American Sub 980 G=0.824 T=0.176
1000Genomes Global Study-wide 5008 G=0.7502 T=0.2498
1000Genomes African Sub 1322 G=0.7390 T=0.2610
1000Genomes East Asian Sub 1008 G=0.8641 T=0.1359
1000Genomes Europe Sub 1006 G=0.7396 T=0.2604
1000Genomes South Asian Sub 978 G=0.608 T=0.392
1000Genomes American Sub 694 G=0.821 T=0.179
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7565 T=0.2435
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7289 T=0.2711
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7460 T=0.2540
KOREAN population from KRGDB KOREAN Study-wide 2922 G=0.8491 T=0.1509
Korean Genome Project KOREAN Study-wide 1832 G=0.8695 T=0.1305
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.769 T=0.231
CNV burdens in cranial meningiomas Global Study-wide 792 G=0.872 T=0.128
CNV burdens in cranial meningiomas CRM Sub 792 G=0.872 T=0.128
Northern Sweden ACPOP Study-wide 600 G=0.785 T=0.215
SGDP_PRJ Global Study-wide 238 G=0.395 T=0.605
Qatari Global Study-wide 216 G=0.565 T=0.435
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.877 T=0.123
The Danish reference pan genome Danish Study-wide 40 G=0.68 T=0.33
Siberian Global Study-wide 14 G=0.50 T=0.50
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 4 NC_000004.12:g.99574331G>A
GRCh38.p14 chr 4 NC_000004.12:g.99574331G>T
GRCh37.p13 chr 4 NC_000004.11:g.100495488G>A
GRCh37.p13 chr 4 NC_000004.11:g.100495488G>T
MTTP RefSeqGene NG_011469.1:g.15249G>A
MTTP RefSeqGene NG_011469.1:g.15249G>T
Gene: MTTP, microsomal triglyceride transfer protein (plus strand)
Molecule type Change Amino acid[Codon] SO Term
MTTP transcript variant 1 NM_000253.4:c.-101-478G>A N/A Intron Variant
MTTP transcript variant 2 NM_001300785.2:c.-188-757…

NM_001300785.2:c.-188-7574G>A

N/A Intron Variant
MTTP transcript variant 3 NM_001386140.1:c. N/A Genic Upstream Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: T (allele ID: 1154870 )
ClinVar Accession Disease Names Clinical Significance
RCV001519435.4 not provided Benign
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A T
GRCh38.p14 chr 4 NC_000004.12:g.99574331= NC_000004.12:g.99574331G>A NC_000004.12:g.99574331G>T
GRCh37.p13 chr 4 NC_000004.11:g.100495488= NC_000004.11:g.100495488G>A NC_000004.11:g.100495488G>T
MTTP RefSeqGene NG_011469.1:g.15249= NG_011469.1:g.15249G>A NG_011469.1:g.15249G>T
MTTP transcript NM_000253.2:c.-101-478= NM_000253.2:c.-101-478G>A NM_000253.2:c.-101-478G>T
MTTP transcript variant 1 NM_000253.4:c.-101-478= NM_000253.4:c.-101-478G>A NM_000253.4:c.-101-478G>T
MTTP transcript variant 2 NM_001300785.2:c.-188-7574= NM_001300785.2:c.-188-7574G>A NM_001300785.2:c.-188-7574G>T
MTTP transcript variant X1 XM_005263025.1:c.143-7574= XM_005263025.1:c.143-7574G>A XM_005263025.1:c.143-7574G>T
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

71 SubSNP, 22 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 HGBASE ss2420700 Nov 14, 2000 (89)
2 PERLEGEN ss24365748 Sep 20, 2004 (123)
3 KYUGEN ss28459258 Sep 20, 2004 (123)
4 BGI ss104099140 Dec 01, 2009 (131)
5 1000GENOMES ss108172872 Jan 23, 2009 (130)
6 ILLUMINA-UK ss117114494 Feb 14, 2009 (130)
7 COMPLETE_GENOMICS ss162382333 Jul 04, 2010 (132)
8 BUSHMAN ss198924034 Jul 04, 2010 (132)
9 1000GENOMES ss221099936 Jul 14, 2010 (132)
10 1000GENOMES ss232516167 Jul 14, 2010 (132)
11 1000GENOMES ss239780869 Jul 15, 2010 (132)
12 ILLUMINA ss244285034 Jul 04, 2010 (132)
13 BL ss253374069 May 09, 2011 (134)
14 GMI ss277845444 May 04, 2012 (137)
15 TISHKOFF ss557722881 Apr 25, 2013 (138)
16 SSMP ss651527210 Apr 25, 2013 (138)
17 EVA-GONL ss980452976 Aug 21, 2014 (142)
18 JMKIDD_LAB ss1071789128 Aug 21, 2014 (142)
19 1000GENOMES ss1310988613 Aug 21, 2014 (142)
20 DDI ss1429983723 Apr 01, 2015 (144)
21 EVA_GENOME_DK ss1580688709 Apr 01, 2015 (144)
22 EVA_DECODE ss1589957106 Apr 01, 2015 (144)
23 EVA_UK10K_ALSPAC ss1610741672 Apr 01, 2015 (144)
24 EVA_UK10K_TWINSUK ss1653735705 Apr 01, 2015 (144)
25 HAMMER_LAB ss1801912938 Sep 08, 2015 (146)
26 WEILL_CORNELL_DGM ss1923692790 Feb 12, 2016 (147)
27 ILLUMINA ss1958707197 Feb 12, 2016 (147)
28 GENOMED ss1969817473 Jul 19, 2016 (147)
29 JJLAB ss2022432594 Sep 14, 2016 (149)
30 USC_VALOUEV ss2150561800 Dec 20, 2016 (150)
31 HUMAN_LONGEVITY ss2265444455 Dec 20, 2016 (150)
32 SYSTEMSBIOZJU ss2625715244 Nov 08, 2017 (151)
33 GRF ss2706038368 Nov 08, 2017 (151)
34 GNOMAD ss2812880408 Nov 08, 2017 (151)
35 SWEGEN ss2995214474 Nov 08, 2017 (151)
36 ILLUMINA ss3022398859 Nov 08, 2017 (151)
37 BIOINF_KMB_FNS_UNIBA ss3024991612 Nov 08, 2017 (151)
38 CSHL ss3345863115 Nov 08, 2017 (151)
39 ILLUMINA ss3652885122 Oct 12, 2018 (152)
40 EGCUT_WGS ss3663110658 Jul 13, 2019 (153)
41 EVA_DECODE ss3712661530 Jul 13, 2019 (153)
42 ILLUMINA ss3726155931 Jul 13, 2019 (153)
43 ACPOP ss3731424175 Jul 13, 2019 (153)
44 EVA ss3762169583 Jul 13, 2019 (153)
45 PAGE_CC ss3771142759 Jul 13, 2019 (153)
46 KHV_HUMAN_GENOMES ss3805317991 Jul 13, 2019 (153)
47 EVA ss3828705007 Apr 26, 2020 (154)
48 EVA ss3837793656 Apr 26, 2020 (154)
49 EVA ss3843232062 Apr 26, 2020 (154)
50 SGDP_PRJ ss3859615437 Apr 26, 2020 (154)
51 KRGDB ss3905892766 Apr 26, 2020 (154)
52 KOGIC ss3954746089 Apr 26, 2020 (154)
53 EVA ss3984532319 Apr 26, 2021 (155)
54 TOPMED ss4624722547 Apr 26, 2021 (155)
55 TOMMO_GENOMICS ss5167087775 Apr 26, 2021 (155)
56 EVA ss5237353874 Apr 26, 2021 (155)
57 1000G_HIGH_COVERAGE ss5260295967 Oct 13, 2022 (156)
58 HUGCELL_USP ss5458937762 Oct 13, 2022 (156)
59 EVA ss5507642659 Oct 13, 2022 (156)
60 1000G_HIGH_COVERAGE ss5541967884 Oct 13, 2022 (156)
61 SANFORD_IMAGENETICS ss5624562766 Oct 13, 2022 (156)
62 SANFORD_IMAGENETICS ss5635670233 Oct 13, 2022 (156)
63 TOMMO_GENOMICS ss5701821746 Oct 13, 2022 (156)
64 YY_MCH ss5805355852 Oct 13, 2022 (156)
65 EVA ss5844427694 Oct 13, 2022 (156)
66 EVA ss5847247792 Oct 13, 2022 (156)
67 EVA ss5848019433 Oct 13, 2022 (156)
68 EVA ss5854357167 Oct 13, 2022 (156)
69 EVA ss5864685842 Oct 13, 2022 (156)
70 EVA ss5964061243 Oct 13, 2022 (156)
71 EVA ss5979708826 Oct 13, 2022 (156)
72 1000Genomes NC_000004.11 - 100495488 Oct 12, 2018 (152)
73 1000Genomes_30x NC_000004.12 - 99574331 Oct 13, 2022 (156)
74 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 100495488 Oct 12, 2018 (152)
75 Genetic variation in the Estonian population NC_000004.11 - 100495488 Oct 12, 2018 (152)
76 The Danish reference pan genome NC_000004.11 - 100495488 Apr 26, 2020 (154)
77 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 158900527 (NC_000004.12:99574330:G:A 2/140082)
Row 158900528 (NC_000004.12:99574330:G:T 36524/140044)

- Apr 26, 2021 (155)
78 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 158900527 (NC_000004.12:99574330:G:A 2/140082)
Row 158900528 (NC_000004.12:99574330:G:T 36524/140044)

- Apr 26, 2021 (155)
79 Genome of the Netherlands Release 5 NC_000004.11 - 100495488 Apr 26, 2020 (154)
80 KOREAN population from KRGDB NC_000004.11 - 100495488 Apr 26, 2020 (154)
81 Korean Genome Project NC_000004.12 - 99574331 Apr 26, 2020 (154)
82 Northern Sweden NC_000004.11 - 100495488 Jul 13, 2019 (153)
83 The PAGE Study NC_000004.12 - 99574331 Jul 13, 2019 (153)
84 CNV burdens in cranial meningiomas NC_000004.11 - 100495488 Apr 26, 2021 (155)
85 Qatari NC_000004.11 - 100495488 Apr 26, 2020 (154)
86 SGDP_PRJ NC_000004.11 - 100495488 Apr 26, 2020 (154)
87 Siberian NC_000004.11 - 100495488 Apr 26, 2020 (154)
88 8.3KJPN NC_000004.11 - 100495488 Apr 26, 2021 (155)
89 14KJPN NC_000004.12 - 99574331 Oct 13, 2022 (156)
90 TopMed NC_000004.12 - 99574331 Apr 26, 2021 (155)
91 UK 10K study - Twins NC_000004.11 - 100495488 Oct 12, 2018 (152)
92 A Vietnamese Genetic Variation Database NC_000004.11 - 100495488 Jul 13, 2019 (153)
93 ALFA NC_000004.12 - 99574331 Apr 26, 2021 (155)
94 ClinVar RCV001519435.4 Oct 13, 2022 (156)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs17598205 Oct 07, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
11908310861 NC_000004.12:99574330:G:A NC_000004.12:99574330:G:A (self)
ss108172872, ss117114494, ss162382333, ss198924034, ss253374069, ss277845444, ss1589957106 NC_000004.10:100714510:G:T NC_000004.12:99574330:G:T (self)
22431134, 12478362, 8848906, 6853648, 5516409, 13070160, 4709040, 81680, 5734720, 11632417, 3078154, 25057082, 12478362, 2745588, ss221099936, ss232516167, ss239780869, ss557722881, ss651527210, ss980452976, ss1071789128, ss1310988613, ss1429983723, ss1580688709, ss1610741672, ss1653735705, ss1801912938, ss1923692790, ss1958707197, ss1969817473, ss2022432594, ss2150561800, ss2625715244, ss2706038368, ss2812880408, ss2995214474, ss3022398859, ss3345863115, ss3652885122, ss3663110658, ss3731424175, ss3762169583, ss3828705007, ss3837793656, ss3859615437, ss3905892766, ss3984532319, ss5167087775, ss5237353874, ss5507642659, ss5624562766, ss5635670233, ss5844427694, ss5847247792, ss5848019433, ss5964061243, ss5979708826 NC_000004.11:100495487:G:T NC_000004.12:99574330:G:T (self)
RCV001519435.4, 29493819, 11124090, 364228, 35658850, 462100103, 11908310861, ss2265444455, ss3024991612, ss3712661530, ss3726155931, ss3771142759, ss3805317991, ss3843232062, ss3954746089, ss4624722547, ss5260295967, ss5458937762, ss5541967884, ss5701821746, ss5805355852, ss5854357167, ss5864685842 NC_000004.12:99574330:G:T NC_000004.12:99574330:G:T (self)
ss2420700, ss24365748, ss28459258, ss104099140, ss244285034 NT_016354.19:25043208:G:T NC_000004.12:99574330:G:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

17 citations for rs1800591
PMID Title Author Year Journal
14615589 Haplotype-based identification of a microsomal transfer protein marker associated with the human lifespan. Geesaman BJ et al. 2003 Proceedings of the National Academy of Sciences of the United States of America
17854051 Functional analysis of promoter variants in the microsomal triglyceride transfer protein (MTTP) gene. Rubin D et al. 2008 Human mutation
19546343 Allele-specific regulation of MTTP expression influences the risk of ischemic heart disease. Aminoff A et al. 2010 Journal of lipid research
23273182 Microsomal triglyceride transfer protein gene -493G/T polymorphism and its association with serum lipid levels in Bama Zhuang long-living families in China. Pan SL et al. 2012 Lipids in health and disease
23533563 Novel risk factors for premature peripheral arterial occlusive disease in non-diabetic patients: a case-control study. Bérard AM et al. 2013 PloS one
23609384 Genetic variants of microsomal triglyceride transfer protein (MTTP) are associated with metabolic syndrome in schizophrenic patients treated with atypical antipsychotics. Liou YJ et al. 2013 Journal of clinical psychopharmacology
24588800 MTP -493G>T polymorphism and susceptibility to nonalcoholic fatty liver disease: a meta-analysis. Zheng W et al. 2014 DNA and cell biology
25368670 CardioGxE, a catalog of gene-environment interactions for cardiometabolic traits. Parnell LD et al. 2014 BioData mining
25587205 Association of polymorphisms of genes involved in lipid metabolism with blood pressure and lipid values in mexican hypertensive individuals. Ríos-González BE et al. 2014 Disease markers
26965314 Gene polymorphisms associated with non-alcoholic fatty liver disease and coronary artery disease: a concise review. Li XL et al. 2016 Lipids in health and disease
27458502 Genetics of non-alcoholic fatty liver disease: From susceptibility and nutrient interactions to management. Ravi Kanth VV et al. 2016 World journal of hepatology
27853387 Treatment-resistant schizophrenia: current insights on the pharmacogenomics of antipsychotics. Lally J et al. 2016 Pharmacogenomics and personalized medicine
29016630 Association between kidney function and genetic polymorphisms in atherosclerotic and chronic kidney diseases: A cross-sectional study in Japanese male workers. Kubo Y et al. 2017 PloS one
29705673 ACE, APOA5, and MTP Gene Polymorphisms Analysis in Relation to Triglyceride and Insulin Levels in Pediatric Patients. Carranza-González L et al. 2018 Archives of medical research
32147132 The influence of gene-chronic hepatitis C virus infection on hepatic fibrosis and steatosis. Magri MC et al. 2020 Diagnostic microbiology and infectious disease
32719241 The association between SNPs rs1800591 and rs3816873 of the MTTP gene and nonalcoholic fatty liver disease: A meta-analysis. Tan J et al. 2020 Saudi journal of gastroenterology
36027755 Effect of MTTP -493G/T, I128T, Q95H and Q244E polymorphisms on hepatic steatosis in patients with chronic hepatitis. Prata TVG et al. 2022 Clinics (Sao Paulo, Brazil)
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07