ClinVar Genomic variation as it relates to human health
GRCh38/hg38 9q33.2(chr9:122546532-122628235)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 | |||
OR1B1 | - | - | - |
GRCh38 GRCh37 |
15 | 46 |
OR1J2 | - | - | - |
GRCh38 GRCh37 |
6 | 135 |
OR1L8 | - | - | - |
GRCh38 GRCh37 |
- | 64 |
OR1N2 | - | - | - |
GRCh38 GRCh37 |
- | 49 |
OR1Q1 | - | - | - |
GRCh38 GRCh37 |
14 | 45 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Apr 30, 2011 | RCV000140625.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023