ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6q23.2(chr6:132859724-132910636)x1
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 | |||
TAAR5 | - | - |
GRCh38 GRCh37 |
33 | 47 | |
TAAR6 | - | - |
GRCh38 GRCh37 |
20 | 34 | |
TAAR8 | - | - |
GRCh38 GRCh37 |
29 | 42 | |
TAAR9 | - | - |
GRCh38 GRCh37 |
31 | 44 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
- | RCV000446076.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024