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rs34968276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34968276(A;A)
Make rs34968276(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971110
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs34968276
dbSNP (classic)rs34968276
ClinGenrs34968276
ebirs34968276
HLIrs34968276
Exacrs34968276
Gnomadrs34968276
Varsomers34968276
LitVarrs34968276
Maprs34968276
PheGenIrs34968276
Biobankrs34968276
1000 genomesrs34968276
hgdprs34968276
ensemblrs34968276
geneviewrs34968276
scholarrs34968276
googlers34968276
pharmgkbrs34968276
gwascentralrs34968276
openSNPrs34968276
23andMers34968276
23andMe allrs34968276
SNPshotrs34968276
SNPdbers34968276
MSV3drs34968276
GWAS Ctlgrs34968276
Max Magnitude0
ClinVar
Risk rs34968276(A;A) rs34968276(G;G)
Alt rs34968276(A;A) rs34968276(G;G)
Reference Rs34968276(C;C)
Significance Probable-Pathogenic
Disease Adenocarcinoma of stomach Malignant melanoma of skin Adenocarcinoma of lung Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Transitional cell carcinoma of the bladder Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Hereditary cancer-predisposing syndrome
Variation info
Gene CDKN2A
CLNDBN Adenocarcinoma of stomach Malignant melanoma of skin Adenocarcinoma of lung Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Transitional cell carcinoma of the bladder Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.21971109G>C; NC_000009.11:g.21971109G>T
CLNSRC
CLNACC RCV000422116.1, RCV000422956.1, RCV000423602.1, RCV000431254.1, RCV000432376.1, RCV000433889.1, RCV000441491.1, RCV000443430.1, RCV000493314.1,