Annotation Detail
Information
- Associated Genes
- PDCD1
- Associated Variants
-
PDCD1 c.627+189G>A
(
ENST00000334409.10 )
PDCD1 c.627+189G>A ( ENST00000334409.10 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_005018.3(PDCD1):c.627+189G>A AND not provided
- ClinVar Allele ID
- 1255474
- ClinVar RefSeq Alternation Syntax
- NM_005018.3:c.627+189G>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/RCV001677921
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs