ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p11.12(chr11:49604582-50596467)x3
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 | |||
OR4C12 | - | - | - |
GRCh38 GRCh38 GRCh37 |
23 | 32 |
OR4C13 | - | - | - |
GRCh38 GRCh37 |
36 | 45 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Sep 22, 2014 | RCV000510928.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024