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rs1057519881

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519881(A;G)
Make rs1057519881(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971111
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs1057519881
dbSNP (old)rs1057519881
ClinGenrs1057519881
ebirs1057519881
HLIrs1057519881
Exacrs1057519881
Gnomadrs1057519881
Varsomers1057519881
Maprs1057519881
PheGenIrs1057519881
Biobankrs1057519881
1000 genomesrs1057519881
hgdprs1057519881
ensemblrs1057519881
gopubmedrs1057519881
geneviewrs1057519881
scholarrs1057519881
googlers1057519881
pharmgkbrs1057519881
gwascentralrs1057519881
openSNPrs1057519881
23andMers1057519881
23andMe allrs1057519881
SNPshotrs1057519881
SNPdbers1057519881
MSV3drs1057519881
GWAS Ctlgrs1057519881
Max Magnitude0
ClinVar
Risk rs1057519881(G;G)
Alt rs1057519881(G;G)
Reference Rs1057519881(A;A)
Significance Probable-Pathogenic
Disease Transitional cell carcinoma of the bladder Squamous cell carcinoma of the skin Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Malignant melanoma of skin Adenocarcinoma of stomach Adenocarcinoma of lung Pancreatic adenocarcinoma
Variation info
Gene CDKN2A
CLNDBN Transitional cell carcinoma of the bladder Squamous cell carcinoma of the skin Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Malignant melanoma of skin Adenocarcinoma of stomach Adenocarcinoma of lung Pancreatic adenocarcinoma
Reversed 1
HGVS NC_000009.11:g.21971110T>C
CLNSRC
CLNACC RCV000418529.1, RCV000426834.1, RCV000427609.1, RCV000433507.1, RCV000434118.1, RCV000437058.1, RCV000442368.1, RCV000442465.1,