ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6p21.33(chr6:31413982-31477904)x1
Germline
Classification
(1)
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 | |||
HCG26 | - | - | - |
GRCh38 GRCh38 GRCh38 GRCh38 GRCh38 GRCh38 GRCh37 |
- | 11 |
HCP5 | - | - |
GRCh38 GRCh38 GRCh38 GRCh38 GRCh37 |
- | 12 | |
LINC01149 | - | - | - |
GRCh38 GRCh38 GRCh38 GRCh38 |
- | 3 |
LOC121132677 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 3 |
MICA | - | - |
GRCh38 GRCh38 GRCh38 GRCh38 GRCh38 GRCh37 |
22 | 33 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Mar 8, 2011 | RCV000136325.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024