Annotation Detail
Information
- Associated Genes
- CYP2R1
- Associated Variants
-
CYP2R1 p.Ser59= (p.S59=)
(
ENST00000334636.10 )
CYP2R1 p.Ser59= (p.S59=) ( ENST00000334636.10 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_024514.5(CYP2R1):c.177C>T (p.Ser59=) AND not specified
- ClinVar Allele ID
- 1156655
- ClinVar RefSeq Alternation Syntax
- NM_024514.5:c.177C>T
- Clinical Significance Description
- Benign
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001528996
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs