ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q31.1(chr7:112984974-113485283)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
GPR85 | - | - |
GRCh38 GRCh37 |
28 | 54 | |
HRAT17 | - | - | - | GRCh38 | - | 4 |
LOC129999145 | - | - | - | GRCh38 | - | 4 |
SMIM30 | - | - | - | GRCh38 | - | 4 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Oct 15, 2012 | RCV000143350.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024