Annotation Detail
Information
- Associated Genes
- TERF2
- Associated Variants
-
TERF2 c.1341-42T>C
(
ENST00000254942.8 )
TERF2 c.1341-42T>C ( ENST00000254942.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_005652.5(TERF2):c.1341-42T>C AND not provided
- ClinVar Allele ID
- 1215287
- ClinVar RefSeq Alternation Syntax
- NM_005652.5:c.1341-42T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001613986
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs