ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9q33.2(chr9:125154228-125339689)x1
Germline
Classification
(1)
Likely 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 | |||
OR1J1 | - | - | - |
GRCh38 GRCh37 |
- | 54 |
OR1J2 | - | - | - |
GRCh38 GRCh37 |
6 | 152 |
OR1J4 | - | - | - |
GRCh38 GRCh37 |
- | 56 |
OR1L8 | - | - | - |
GRCh38 GRCh37 |
- | 68 |
OR1N1 | - | - | - |
GRCh38 GRCh37 |
- | 58 |
OR1N2 | - | - | - |
GRCh38 GRCh37 |
- | 52 |
PTGS1 | - | - |
GRCh38 GRCh37 |
37 | 73 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
May 4, 2020 | RCV001259051.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022