Annotation Detail
Information
- Associated Genes
- SRD5A2
- Associated Variants
-
SRD5A2 p.Gln48= (p.Q48=)
(
ENST00000622030.2 )
SRD5A2 p.Ala49Thr (p.A49T) ( ENST00000622030.2 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000348.4(SRD5A2):c.145G>A (p.Ala49Thr) AND not provided
- ClinVar Allele ID
- 18386
- ClinVar RefSeq Alternation Syntax
- NM_000348.4:c.145G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2015-03-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000083640
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- not provided
Drugs