ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6p24.3-24.2(chr6:10564018-10629482)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 | |||
GCNT2 | - | - |
GRCh38 GRCh38 GRCh37 |
195 | 236 | |
LOC123575665 | - | - | - |
GRCh38 GRCh38 |
- | 15 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Nov 30, 2010 | RCV000135238.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022