Annotation Detail
Information
- Associated Genes
- MLH1
- Associated Variants
-
MLH1 c.-93G>A
(
ENST00000536378.5,
ENST00000673673.2 )
MLH1 c.-93G>A ( ENST00000536378.5, ENST00000673673.2 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000249.3(MLH1):c.-93G>A AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 95074
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2014-11-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000215209
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs