Name: rs885883
Published: September 21, 2022
License: Open Access

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.

rs885883

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:106865837 (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: T>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.397125 (118830/299226, ALFA)
C=0.307548 (81405/264690, TOPMED)
C=0.29740 (23383/78626, PAGE_STUDY) (+ 3 more)
T=0.46044 (13011/28258, 14KJPN)
C=0.4803 (880/1832, Korea1K)
C=0.2803 (499/1780, HapMap)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC124903399 : Non Coding Transcript Variant
Publications: 1 citation
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	304228	T=0.604182	A=0.000000, C=0.395818, G=0.000000
European	Sub	265114	T=0.594544	A=0.000000, C=0.405456, G=0.000000
African	Sub	9788	T=0.9405	A=0.0000, C=0.0595, G=0.0000
African Others	Sub	380	T=0.992	A=0.000, C=0.008, G=0.000
African American	Sub	9408	T=0.9385	A=0.0000, C=0.0615, G=0.0000
Asian	Sub	3880	T=0.5162	A=0.0000, C=0.4838, G=0.0000
East Asian	Sub	3124	T=0.5464	A=0.0000, C=0.4536, G=0.0000
Other Asian	Sub	756	T=0.392	A=0.000, C=0.608, G=0.000
Latin American 1	Sub	1196	T=0.7065	A=0.0000, C=0.2935, G=0.0000
Latin American 2	Sub	8938	T=0.5126	A=0.0000, C=0.4874, G=0.0000
South Asian	Sub	5176	T=0.6329	A=0.0000, C=0.3671, G=0.0000
Other	Sub	10136	T=0.61908	A=0.00000, C=0.38092, G=0.00000

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	299226	T=0.602762	A=0.000000, C=0.397125, G=0.000000
Allele Frequency Aggregator	European	Sub	262054	T=0.594370	A=0.000000, C=0.405500, G=0.000000
Allele Frequency Aggregator	Other	Sub	9336	T=0.6173	A=0.0000, C=0.3827, G=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	8938	T=0.5126	A=0.0000, C=0.4874, G=0.0000
Allele Frequency Aggregator	African	Sub	8646	T=0.9410	A=0.0000, C=0.0590, G=0.0000
Allele Frequency Aggregator	South Asian	Sub	5176	T=0.6329	A=0.0000, C=0.3671, G=0.0000
Allele Frequency Aggregator	Asian	Sub	3880	T=0.5162	A=0.0000, C=0.4838, G=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	1196	T=0.7065	A=0.0000, C=0.2935, G=0.0000
TopMed	Global	Study-wide	264690	T=0.692452	C=0.307548
The PAGE Study	Global	Study-wide	78626	T=0.70260	C=0.29740
The PAGE Study	AfricanAmerican	Sub	32508	T=0.90962	C=0.09038
The PAGE Study	Mexican	Sub	10800	T=0.49963	C=0.50037
The PAGE Study	Asian	Sub	8272	T=0.4648	C=0.5352
The PAGE Study	PuertoRican	Sub	7916	T=0.6450	C=0.3550
The PAGE Study	NativeHawaiian	Sub	4532	T=0.4684	C=0.5316
The PAGE Study	Cuban	Sub	4228	T=0.6351	C=0.3649
The PAGE Study	Dominican	Sub	3828	T=0.7534	C=0.2466
The PAGE Study	CentralAmerican	Sub	2448	T=0.5037	C=0.4963
The PAGE Study	SouthAmerican	Sub	1982	T=0.5545	C=0.4455
The PAGE Study	NativeAmerican	Sub	1258	T=0.6232	C=0.3768
The PAGE Study	SouthAsian	Sub	854	T=0.607	C=0.393
14KJPN	JAPANESE	Study-wide	28258	T=0.46044	C=0.53956
Korean Genome Project	KOREAN	Study-wide	1832	T=0.5197	C=0.4803
HapMap	Global	Study-wide	1780	T=0.7197	C=0.2803
HapMap	American	Sub	766	T=0.650	C=0.350
HapMap	African	Sub	586	T=0.974	C=0.026
HapMap	Asian	Sub	254	T=0.441	C=0.559
HapMap	Europe	Sub	174	T=0.575	C=0.425

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 14	NC_000014.9:g.106865837T>A
GRCh38.p14 chr 14	NC_000014.9:g.106865837T>C
GRCh38.p14 chr 14	NC_000014.9:g.106865837T>G
GRCh37.p13 chr 14	NC_000014.8:g.107274052C>T
GRCh37.p13 chr 14	NC_000014.8:g.107274052C>A
GRCh37.p13 chr 14	NC_000014.8:g.107274052C>G
IGH genomic region	NG_001019.6:g.14508A>T
IGH genomic region	NG_001019.6:g.14508A>G
IGH genomic region	NG_001019.6:g.14508A>C

Gene: LOC124903399, uncharacterized LOC124903399 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903399 transcript variant X1	XR_007064370.1:n.1744T>A	N/A	Non Coding Transcript Variant
LOC124903399 transcript variant X1	XR_007064370.1:n.1744T>C	N/A	Non Coding Transcript Variant
LOC124903399 transcript variant X1	XR_007064370.1:n.1744T>G	N/A	Non Coding Transcript Variant

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.

Not Reported in ClinVar

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	T=	A	C	G
GRCh38.p14 chr 14	NC_000014.9:g.106865837=	NC_000014.9:g.106865837T>A	NC_000014.9:g.106865837T>C	NC_000014.9:g.106865837T>G
GRCh37.p13 chr 14	NC_000014.8:g.107274052C>T	NC_000014.8:g.107274052C>A	NC_000014.8:g.107274052=	NC_000014.8:g.107274052C>G
IGH genomic region	NG_001019.6:g.14508=	NG_001019.6:g.14508A>T	NG_001019.6:g.14508A>G	NG_001019.6:g.14508A>C
LOC124903399 transcript variant X1	XR_007064370.1:n.1744=	XR_007064370.1:n.1744T>A	XR_007064370.1:n.1744T>C	XR_007064370.1:n.1744T>G

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#.

153 SubSNP, 8 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1313553	Oct 05, 2000 (86)
2	SC_JCM	ss6049095	Feb 20, 2003 (111)
3	CSHL-HAPMAP	ss17523189	Feb 27, 2004 (120)
4	SSAHASNP	ss21177540	Apr 05, 2004 (121)
5	PERLEGEN	ss24120152	Sep 20, 2004 (123)
6	AFFY	ss66532765	Dec 01, 2006 (127)
7	ILLUMINA	ss66759241	Dec 01, 2006 (127)
8	ILLUMINA	ss67887640	Dec 01, 2006 (127)
9	ILLUMINA	ss68025694	Dec 01, 2006 (127)
10	ILLUMINA	ss70978463	May 23, 2008 (130)
11	ILLUMINA	ss71590332	May 18, 2007 (127)
12	ILLUMINA	ss75613396	Dec 07, 2007 (129)
13	AFFY	ss76355197	Dec 07, 2007 (129)
14	ILLUMINA	ss79286751	Dec 14, 2007 (130)
15	HGSV	ss81070573	Dec 14, 2007 (130)
16	KRIBB_YJKIM	ss83594550	Dec 14, 2007 (130)
17	BCMHGSC_JDW	ss90077760	Mar 24, 2008 (129)
18	HUMANGENOME_JCVI	ss96887320	Feb 04, 2009 (130)
19	BGI	ss106415436	Feb 04, 2009 (130)
20	1000GENOMES	ss108653668	Jan 23, 2009 (130)
21	1000GENOMES	ss113877136	Jan 25, 2009 (130)
22	ILLUMINA-UK	ss118819416	Feb 14, 2009 (130)
23	ILLUMINA	ss122934377	Dec 01, 2009 (131)
24	ENSEMBL	ss134174968	Dec 01, 2009 (131)
25	ENSEMBL	ss143897462	Dec 01, 2009 (131)
26	ILLUMINA	ss154477661	Dec 01, 2009 (131)
27	ILLUMINA	ss159652094	Dec 01, 2009 (131)
28	ILLUMINA	ss160962793	Dec 01, 2009 (131)
29	COMPLETE_GENOMICS	ss168650736	Jul 04, 2010 (132)
30	COMPLETE_GENOMICS	ss170701146	Jul 04, 2010 (132)
31	COMPLETE_GENOMICS	ss171694276	Jul 04, 2010 (132)
32	ILLUMINA	ss172421024	Jul 04, 2010 (132)
33	AFFY	ss173366196	Jul 04, 2010 (132)
34	ILLUMINA	ss174766725	Jul 04, 2010 (132)
35	BUSHMAN	ss200573903	Jul 04, 2010 (132)
36	BCM-HGSC-SUB	ss206874630	Jul 04, 2010 (132)
37	1000GENOMES	ss226787811	Jul 14, 2010 (132)
38	1000GENOMES	ss236703316	Jul 15, 2010 (132)
39	1000GENOMES	ss243105425	Jul 15, 2010 (132)
40	GMI	ss282159605	May 04, 2012 (137)
41	GMI	ss286911606	Apr 25, 2013 (138)
42	PJP	ss291676200	May 09, 2011 (134)
43	ILLUMINA	ss481825330	May 04, 2012 (137)
44	ILLUMINA	ss481857843	May 04, 2012 (137)
45	ILLUMINA	ss482817146	Sep 08, 2015 (146)
46	ILLUMINA	ss485707192	May 04, 2012 (137)
47	ILLUMINA	ss537570801	Sep 08, 2015 (146)
48	TISHKOFF	ss564349078	Apr 25, 2013 (138)
49	SSMP	ss660051639	Apr 25, 2013 (138)
50	ILLUMINA	ss779002177	Sep 08, 2015 (146)
51	ILLUMINA	ss783299204	Aug 21, 2014 (142)
52	ILLUMINA	ss784251556	Sep 08, 2015 (146)
53	ILLUMINA	ss825617269	Apr 01, 2015 (144)
54	ILLUMINA	ss832560542	Apr 01, 2015 (144)
55	ILLUMINA	ss833162903	Aug 21, 2014 (142)
56	ILLUMINA	ss833753731	Aug 21, 2014 (142)
57	ILLUMINA	ss834464551	Sep 08, 2015 (146)
58	EVA-GONL	ss991571196	Aug 21, 2014 (142)
59	EVA-GONL	ss991571197	Aug 21, 2014 (142)
60	JMKIDD_LAB	ss1079968826	Aug 21, 2014 (142)
61	1000GENOMES	ss1352611837	Aug 21, 2014 (142)
62	1000GENOMES	ss1374622299	Aug 21, 2014 (142)
63	DDI	ss1427551936	Apr 01, 2015 (144)
64	EVA_GENOME_DK	ss1577495994	Apr 01, 2015 (144)
65	EVA_UK10K_ALSPAC	ss1632587085	Apr 01, 2015 (144)
66	EVA_UK10K_TWINSUK	ss1675581118	Apr 01, 2015 (144)
67	EVA_DECODE	ss1695585286	Apr 01, 2015 (144)
68	EVA_DECODE	ss1695585287	Apr 01, 2015 (144)
69	EVA_UK10K_ALSPAC	ss1708212439	Apr 01, 2015 (144)
70	EVA_UK10K_TWINSUK	ss1708212549	Apr 01, 2015 (144)
71	EVA_MGP	ss1711387418	Apr 01, 2015 (144)
72	EVA_SVP	ss1713474543	Apr 01, 2015 (144)
73	ILLUMINA	ss1752122933	Sep 08, 2015 (146)
74	HAMMER_LAB	ss1808103106	Sep 08, 2015 (146)
75	WEILL_CORNELL_DGM	ss1934946675	Feb 12, 2016 (147)
76	ILLUMINA	ss1946387571	Feb 12, 2016 (147)
77	ILLUMINA	ss1959590478	Feb 12, 2016 (147)
78	GENOMED	ss1968057110	Jul 19, 2016 (147)
79	JJLAB	ss2028259414	Sep 14, 2016 (149)
80	USC_VALOUEV	ss2156651450	Dec 20, 2016 (150)
81	SYSTEMSBIOZJU	ss2628619766	Nov 08, 2017 (151)
82	ILLUMINA	ss2633203360	Nov 08, 2017 (151)
83	GRF	ss2701092691	Nov 08, 2017 (151)
84	ILLUMINA	ss2710810725	Nov 08, 2017 (151)
85	GNOMAD	ss2932226218	Nov 08, 2017 (151)
86	GNOMAD	ss2932226219	Nov 08, 2017 (151)
87	SWEGEN	ss3012870874	Nov 08, 2017 (151)
88	ILLUMINA	ss3021608692	Nov 08, 2017 (151)
89	BIOINF_KMB_FNS_UNIBA	ss3027955880	Nov 08, 2017 (151)
90	CSHL	ss3351001771	Nov 08, 2017 (151)
91	ILLUMINA	ss3625668324	Oct 12, 2018 (152)
92	ILLUMINA	ss3627313649	Oct 12, 2018 (152)
93	ILLUMINA	ss3631198013	Oct 12, 2018 (152)
94	ILLUMINA	ss3633090067	Oct 12, 2018 (152)
95	ILLUMINA	ss3633794334	Oct 12, 2018 (152)
96	ILLUMINA	ss3634596055	Oct 12, 2018 (152)
97	ILLUMINA	ss3635483468	Oct 12, 2018 (152)
98	ILLUMINA	ss3636285647	Oct 12, 2018 (152)
99	ILLUMINA	ss3637234676	Oct 12, 2018 (152)
100	ILLUMINA	ss3638073485	Oct 12, 2018 (152)
101	ILLUMINA	ss3639050164	Oct 12, 2018 (152)
102	ILLUMINA	ss3639530174	Oct 12, 2018 (152)
103	ILLUMINA	ss3640303382	Oct 12, 2018 (152)
104	ILLUMINA	ss3641056749	Oct 12, 2018 (152)
105	ILLUMINA	ss3641351863	Oct 12, 2018 (152)
106	ILLUMINA	ss3643058355	Oct 12, 2018 (152)
107	ILLUMINA	ss3644640707	Oct 12, 2018 (152)
108	URBANLAB	ss3650289910	Oct 12, 2018 (152)
109	ILLUMINA	ss3652007831	Oct 12, 2018 (152)
110	EGCUT_WGS	ss3680117687	Jul 13, 2019 (153)
111	EGCUT_WGS	ss3680117688	Jul 13, 2019 (153)
112	EVA_DECODE	ss3697476606	Jul 13, 2019 (153)
113	ILLUMINA	ss3725481215	Jul 13, 2019 (153)
114	ACPOP	ss3740739940	Jul 13, 2019 (153)
115	ACPOP	ss3740739941	Jul 13, 2019 (153)
116	ILLUMINA	ss3744128041	Jul 13, 2019 (153)
117	ILLUMINA	ss3744896645	Jul 13, 2019 (153)
118	EVA	ss3752829222	Jul 13, 2019 (153)
119	PAGE_CC	ss3771816156	Jul 13, 2019 (153)
120	ILLUMINA	ss3772395361	Jul 13, 2019 (153)
121	KHV_HUMAN_GENOMES	ss3818143172	Jul 13, 2019 (153)
122	EVA	ss3834128733	Apr 27, 2020 (154)
123	EVA	ss3840655273	Apr 27, 2020 (154)
124	EVA	ss3846144903	Apr 27, 2020 (154)
125	HGDP	ss3847516754	Apr 27, 2020 (154)
126	SGDP_PRJ	ss3882382466	Apr 27, 2020 (154)
127	KRGDB	ss3931480863	Apr 27, 2020 (154)
128	KOGIC	ss3975702657	Apr 27, 2020 (154)
129	EVA	ss3984697965	Apr 26, 2021 (155)
130	EVA	ss3985704338	Apr 26, 2021 (155)
131	TOPMED	ss4984143830	Apr 26, 2021 (155)
132	TOMMO_GENOMICS	ss5215062447	Apr 26, 2021 (155)
133	1000G_HIGH_COVERAGE	ss5297642352	Oct 16, 2022 (156)
134	EVA	ss5315768362	Oct 16, 2022 (156)
135	EVA	ss5417839083	Oct 16, 2022 (156)
136	HUGCELL_USP	ss5491530874	Oct 16, 2022 (156)
137	EVA	ss5511371451	Oct 16, 2022 (156)
138	SANFORD_IMAGENETICS	ss5624355040	Oct 16, 2022 (156)
139	SANFORD_IMAGENETICS	ss5657031961	Oct 16, 2022 (156)
140	SANFORD_IMAGENETICS	ss5657031962	Oct 16, 2022 (156)
141	TOMMO_GENOMICS	ss5768406601	Oct 16, 2022 (156)
142	EVA	ss5799931741	Oct 16, 2022 (156)
143	YY_MCH	ss5815107997	Oct 16, 2022 (156)
144	EVA	ss5841671279	Oct 16, 2022 (156)
145	EVA	ss5841671280	Oct 16, 2022 (156)
146	EVA	ss5847444961	Oct 16, 2022 (156)
147	EVA	ss5847734970	Oct 16, 2022 (156)
148	EVA	ss5851206757	Oct 16, 2022 (156)
149	EVA	ss5902957598	Oct 16, 2022 (156)
150	EVA	ss5948490204	Oct 16, 2022 (156)
151	EVA	ss5948490205	Oct 16, 2022 (156)
152	EVA	ss5979454020	Oct 16, 2022 (156)
153	EVA	ss5980854274	Oct 16, 2022 (156)
154	gnomAD - Genomes Submission ignored due to conflicting rows: Row 462647815 (NC_000014.9:106865836:T:C 43683/139228) Row 462647816 (NC_000014.9:106865836:T:G 1/139284)	-	Apr 26, 2021 (155)
155	gnomAD - Genomes Submission ignored due to conflicting rows: Row 462647815 (NC_000014.9:106865836:T:C 43683/139228) Row 462647816 (NC_000014.9:106865836:T:G 1/139284)	-	Apr 26, 2021 (155)
156	HapMap	NC_000014.9 - 106865837	Apr 27, 2020 (154)
157	Korean Genome Project	NC_000014.9 - 106865837	Apr 27, 2020 (154)
158	The PAGE Study	NC_000014.9 - 106865837	Jul 13, 2019 (153)
159	14KJPN	NC_000014.9 - 106865837	Oct 16, 2022 (156)
160	TopMed	NC_000014.9 - 106865837	Apr 26, 2021 (155)
161	ALFA	NC_000014.9 - 106865837	Apr 26, 2021 (155)

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)
rs57259752	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10791132142	NC_000014.9:106865836:T:A	NC_000014.9:106865836:T:A	(self)
ss66532765, ss76355197, ss81070573, ss90077760, ss108653668, ss113877136, ss118819416, ss168650736, ss170701146, ss171694276, ss173366196, ss200573903, ss206874630, ss282159605, ss286911606, ss291676200, ss481825330, ss825617269, ss1695585286, ss1695585287, ss1713474543, ss3639050164, ss3639530174, ss3643058355, ss3847516754	NC_000014.7:106345096:C:C	NC_000014.9:106865836:T:C	(self)
ss226787811, ss236703316, ss243105425, ss481857843, ss482817146, ss485707192, ss537570801, ss564349078, ss660051639, ss779002177, ss783299204, ss784251556, ss832560542, ss833162903, ss833753731, ss834464551, ss991571196, ss991571197, ss1079968826, ss1352611837, ss1374622299, ss1427551936, ss1577495994, ss1632587085, ss1675581118, ss1708212439, ss1708212549, ss1711387418, ss1752122933, ss1808103106, ss1934946675, ss1946387571, ss1959590478, ss1968057110, ss2028259414, ss2156651450, ss2628619766, ss2633203360, ss2701092691, ss2710810725, ss2932226218, ss2932226219, ss3012870874, ss3021608692, ss3351001771, ss3625668324, ss3627313649, ss3631198013, ss3633090067, ss3633794334, ss3634596055, ss3635483468, ss3636285647, ss3637234676, ss3638073485, ss3640303382, ss3641056749, ss3641351863, ss3644640707, ss3652007831, ss3680117687, ss3680117688, ss3740739940, ss3740739941, ss3744128041, ss3744896645, ss3752829222, ss3772395361, ss3834128733, ss3840655273, ss3882382466, ss3931480863, ss3984697965, ss3985704338, ss5215062447, ss5315768362, ss5417839083, ss5511371451, ss5624355040, ss5657031961, ss5657031962, ss5799931741, ss5841671279, ss5841671280, ss5847444961, ss5847734970, ss5948490204, ss5948490205, ss5979454020, ss5980854274	NC_000014.8:107274051:C:C	NC_000014.9:106865836:T:C	(self)
1223718, 32080658, 1037625, 102243705, 199689489, 10791132142, ss3027955880, ss3650289910, ss3697476606, ss3725481215, ss3771816156, ss3818143172, ss3846144903, ss3975702657, ss4984143830, ss5297642352, ss5491530874, ss5768406601, ss5815107997, ss5851206757, ss5902957598	NC_000014.9:106865836:T:C	NC_000014.9:106865836:T:C	(self)
ss17523189, ss21177540	NT_026437.10:87175727:C:C	NC_000014.9:106865836:T:C	(self)
ss1313553, ss6049095, ss24120152, ss66759241, ss67887640, ss68025694, ss70978463, ss71590332, ss75613396, ss79286751, ss83594550, ss96887320, ss106415436, ss122934377, ss134174968, ss143897462, ss154477661, ss159652094, ss160962793, ss172421024, ss174766725	NT_026437.12:88274051:C:C	NC_000014.9:106865836:T:C	(self)
10791132142	NC_000014.9:106865836:T:G	NC_000014.9:106865836:T:G	(self)

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

1 citation for rs885883

PMID	Title	Author	Year	Journal
19461586	Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study.	Norris JM et al.	2009	Obesity (Silver Spring, Md.)

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs885883