ClinVar Genomic variation as it relates to human health
NM_005210.4(CRYGB):c.181G>A (p.Gly61Arg)
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 | |||
CRYGB | - | - |
GRCh38 GRCh37 |
- | 79 | |
LOC100507443 | - | - | - |
GRCh38 GRCh38 |
- | 232 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
CRYGB-related disorder
|
Uncertain significance (1) |
|
Apr 29, 2024 | RCV004758424.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 13, 2024