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rs121913385

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913385(C;T)
Make rs121913385(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971112
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913385
dbSNP (old)rs121913385
ClinGenrs121913385
ebirs121913385
HLIrs121913385
Exacrs121913385
Gnomadrs121913385
Varsomers121913385
Maprs121913385
PheGenIrs121913385
Biobankrs121913385
1000 genomesrs121913385
hgdprs121913385
ensemblrs121913385
gopubmedrs121913385
geneviewrs121913385
scholarrs121913385
googlers121913385
pharmgkbrs121913385
gwascentralrs121913385
openSNPrs121913385
23andMers121913385
23andMe allrs121913385
SNPshotrs121913385
SNPdbers121913385
MSV3drs121913385
GWAS Ctlgrs121913385
Max Magnitude0
ClinVar
Risk rs121913385(G;G) rs121913385(T;T)
Alt rs121913385(G;G) rs121913385(T;T)
Reference Rs121913385(C;C)
Significance Probable-Pathogenic
Disease Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Transitional cell carcinoma of the bladder Neoplasm Pancreatic adenocarcinoma Adenocarcinoma of stomach Malignant melanoma of skin Squamous cell carcinoma of the skin Hepatocellular carcinoma
Variation info
Gene CDKN2A
CLNDBN Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Transitional cell carcinoma of the bladder Neoplasm Pancreatic adenocarcinoma Adenocarcinoma of stomach Malignant melanoma of skin Squamous cell carcinoma of the skin Hepatocellular carcinoma
Reversed 1
HGVS NC_000009.11:g.21971111G>A; NC_000009.11:g.21971111G>C
CLNSRC
CLNACC RCV000419112.1, RCV000421013.1, RCV000423848.1, RCV000426295.1, RCV000429387.1, RCV000432117.1, RCV000438754.1, RCV000438919.1, RCV000439424.1, RCV000418136.1, RCV000418718.1, RCV000425239.1, RCV000428114.1, RCV000428379.1, RCV000434935.1, RCV000436374.1, RCV000441259.1,