ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7p22.3(chr7:896276-940377)x3
Germline
Classification
(1)
Benign
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 | |||
ADAP1 | - | - |
GRCh38 GRCh37 |
20 | 79 | |
GET4 | - | - |
GRCh38 GRCh37 |
36 | 90 | |
LOC129997742 | - | - | - | GRCh38 | - | 27 |
LOC129997743 | - | - | - | GRCh38 | - | 27 |
LOC129997744 | - | - | - | GRCh38 | - | 27 |
LOC129997745 | - | - | - | GRCh38 | - | 27 |
LOC129997746 | - | - | - | GRCh38 | - | 27 |
LOC129997747 | - | - | - | GRCh38 | - | 27 |
LOC129997748 | - | - | - | GRCh38 | - | 27 |
LOC129997749 | - | - | - | GRCh38 | - | 27 |
There is 1 more gene affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Apr 30, 2011 | RCV000140261.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023