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rs121913383

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913383(G;T)
Make rs121913383(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971154
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913383
dbSNP (old)rs121913383
ClinGenrs121913383
ebirs121913383
HLIrs121913383
Exacrs121913383
Gnomadrs121913383
Varsomers121913383
Maprs121913383
PheGenIrs121913383
Biobankrs121913383
1000 genomesrs121913383
hgdprs121913383
ensemblrs121913383
gopubmedrs121913383
geneviewrs121913383
scholarrs121913383
googlers121913383
pharmgkbrs121913383
gwascentralrs121913383
openSNPrs121913383
23andMers121913383
23andMe allrs121913383
SNPshotrs121913383
SNPdbers121913383
MSV3drs121913383
GWAS Ctlgrs121913383
Max Magnitude0
ClinVar
Risk rs121913383(T;T)
Alt rs121913383(T;T)
Reference Rs121913383(G;G)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene CDKN2A
CLNDBN Neoplasm
Reversed 1
HGVS NC_000009.11:g.21971153C>A
CLNSRC
CLNACC RCV000436921.1,