Annotation Detail

Information
Associated Genes
PTGS2 PACERR
Associated Variants
NR_125801.1(PACERR):n.536C>G
NR_125801.1(PACERR):n.536C>G
Source Database
ClinVar
Description
NR_125801.1(PACERR):n.536C>G AND Cholangiocarcinoma
ClinVar Allele ID
2736346
ClinVar RefSeq Alternation Syntax
NR_125801.1:n.536C>G
Clinical Significance Description
other
Clinical Significance Last Update
2022-12-10
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV003312794
Observed Origin Sample
germline
Drugs