Annotation Detail
Information
- Associated Genes
- XRCC2
- Associated Variants
-
NC_000007.14:g.152676167C>G
(
ENST00000698506.1 )
NC_000007.14:g.152676167C>G ( ENST00000698506.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000007.14:g.152676167C>G AND not provided
- ClinVar Allele ID
- 1255464
- 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/RCV001677911
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs