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rs121913389

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913389(A;A)
Make rs121913389(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971029
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913389
dbSNP (old)rs121913389
ClinGenrs121913389
ebirs121913389
HLIrs121913389
Exacrs121913389
Gnomadrs121913389
Varsomers121913389
Maprs121913389
PheGenIrs121913389
Biobankrs121913389
1000 genomesrs121913389
hgdprs121913389
ensemblrs121913389
gopubmedrs121913389
geneviewrs121913389
scholarrs121913389
googlers121913389
pharmgkbrs121913389
gwascentralrs121913389
openSNPrs121913389
23andMers121913389
23andMe allrs121913389
SNPshotrs121913389
SNPdbers121913389
MSV3drs121913389
GWAS Ctlgrs121913389
Max Magnitude0
ClinVar
Risk rs121913389(A;A)
Alt rs121913389(A;A)
Reference Rs121913389(G;G)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene CDKN2A
CLNDBN Neoplasm
Reversed 1
HGVS NC_000009.11:g.21971028C>T
CLNSRC
CLNACC RCV000432172.1,