ClinVar Genomic variation as it relates to human health
GRCh38/hg38 9q31.1(chr9:104300531-104730156)x3
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 | |||
LOC126860709 | - | - | - | GRCh38 | - | 22 |
LOC126860710 | - | - | - | GRCh38 | - | 23 |
OR13C2 | - | - | - |
GRCh38 GRCh37 |
23 | 65 |
OR13C3 | - | - | - |
GRCh38 GRCh37 |
25 | 67 |
OR13C4 | - | - | - |
GRCh38 GRCh37 |
22 | 64 |
OR13C5 | - | - | - |
GRCh38 GRCh37 |
29 | 71 |
OR13C8 | - | - | - |
GRCh38 GRCh37 |
20 | 62 |
OR13C9 | - | - | - |
GRCh38 GRCh37 |
10 | 52 |
OR13D1 | - | - | - |
GRCh38 GRCh37 |
17 | 59 |
OR13F1 | - | - | - |
GRCh38 GRCh37 |
28 | 70 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Nov 30, 2010 | RCV000136069.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024