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rs121913382

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913382(G;T)
Make rs121913382(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971178
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913382
dbSNP (old)rs121913382
ClinGenrs121913382
ebirs121913382
HLIrs121913382
Exacrs121913382
Gnomadrs121913382
Varsomers121913382
Maprs121913382
PheGenIrs121913382
Biobankrs121913382
1000 genomesrs121913382
hgdprs121913382
ensemblrs121913382
gopubmedrs121913382
geneviewrs121913382
scholarrs121913382
googlers121913382
pharmgkbrs121913382
gwascentralrs121913382
openSNPrs121913382
23andMers121913382
23andMe allrs121913382
SNPshotrs121913382
SNPdbers121913382
MSV3drs121913382
GWAS Ctlgrs121913382
Max Magnitude0
ClinVar
Risk rs121913382(T;T)
Alt rs121913382(T;T)
Reference Rs121913382(G;G)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene CDKN2A
CLNDBN Neoplasm
Reversed 1
HGVS NC_000009.11:g.21971177C>A
CLNSRC
CLNACC RCV000419719.1,