ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6q23.2(chr6:132951409-133081430)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
TAAR1 | - | - |
GRCh38 GRCh37 |
20 | 37 | |
VNN1 | - | - |
GRCh38 GRCh37 |
37 | 62 | |
VNN2 | - | - |
GRCh38 GRCh37 |
35 | 56 | |
VNN3 | - | - |
GRCh38 GRCh37 |
1 | 18 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003986641.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024