ClinVar Genomic variation as it relates to human health
NM_000044.6(AR):c.1368_1376dup (p.Gly473_Glu474insGlyGlyGly)
Germline
Classification
(2)
Benign/Likely benign
criteria provided, multiple submitters, no conflicts
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 | |||
AR | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
799 | 1007 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Feb 1, 2024 | RCV003884858.3 | |
Benign (1) |
|
Oct 29, 2021 | RCV003984453.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024