Annotation Detail
Information
- Associated Genes
- GSTP1
- Associated Variants
-
GSTP1 c.[313A>G;341=]
(
ENST00000398606.10 )
GSTP1 c.[313A>G;341=] ( ENST00000398606.10 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000852.4(GSTP1):c.313A>G (p.Ile105Val) AND not provided
- ClinVar Allele ID
- 37785
- ClinVar RefSeq Alternation Syntax
- NM_000852.4:c.313A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-06-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001642249
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs