Annotation Detail
Information
- Associated Genes
- GSTP1
- Associated Variants
-
GSTP1 c.232+13C>A
GSTP1 c.232+13C>A - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000852.4(GSTP1):c.232+13C>A AND not provided
- ClinVar Allele ID
- 1287765
- ClinVar RefSeq Alternation Syntax
- NM_000852.4:c.232+13C>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-06-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001725486
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs