ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1q23.1-24.2(chr1:157321299-167391423)x1
Germline
Classification
(1)
Pathogenic
no assertion criteria provided
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
PBX1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
111 | 131 | |
SDHC | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
848 | 890 | |
ACKR1 | - | - |
GRCh38 GRCh37 |
22 | 32 | |
ADAMTS4 | - | - |
GRCh38 GRCh37 |
44 | 81 | |
AIM2 | - | - |
GRCh38 GRCh37 |
22 | 32 | |
ALDH9A1 | - | - |
GRCh38 GRCh37 |
29 | 49 | |
APCS | - | - |
GRCh38 GRCh37 |
12 | 22 | |
APOA2 | - | - |
GRCh38 GRCh37 |
28 | 47 | |
ARHGAP30 | - | - |
GRCh38 GRCh37 |
54 | 72 | |
ATF6 | - | - |
GRCh38 GRCh37 |
426 | 446 |
There are 124 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
May 2, 2017 | RCV000848773.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023