ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9q33.2(chr9:125105375-125616987)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 | |||
OR1B1 | - | - | - |
GRCh38 GRCh37 |
15 | 46 |
OR1J1 | - | - | - |
GRCh38 GRCh37 |
- | 50 |
OR1J2 | - | - | - |
GRCh38 GRCh37 |
6 | 135 |
OR1J4 | - | - | - |
GRCh38 GRCh37 |
- | 51 |
OR1K1 | - | - | - |
GRCh38 GRCh37 |
25 | 56 |
OR1L1 | - | - | - |
GRCh38 GRCh37 |
13 | 43 |
OR1L3 | - | - | - |
GRCh38 GRCh37 |
18 | 48 |
OR1L4 | - | - | - |
GRCh38 GRCh37 |
24 | 54 |
OR1L6 | - | - | - |
GRCh38 GRCh37 |
20 | 50 |
OR1L8 | - | - | - |
GRCh38 GRCh37 |
- | 64 |
There are 7 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 24, 2019 | RCV001006271.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023