Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913387

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913387(C;T)
Make rs121913387(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971187
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913387
dbSNP (old)rs121913387
ClinGenrs121913387
ebirs121913387
HLIrs121913387
Exacrs121913387
Gnomadrs121913387
Varsomers121913387
LitVarrs121913387
Maprs121913387
PheGenIrs121913387
Biobankrs121913387
1000 genomesrs121913387
hgdprs121913387
ensemblrs121913387
gopubmedrs121913387
geneviewrs121913387
scholarrs121913387
googlers121913387
pharmgkbrs121913387
gwascentralrs121913387
openSNPrs121913387
23andMers121913387
23andMe allrs121913387
SNPshotrs121913387
SNPdbers121913387
MSV3drs121913387
GWAS Ctlgrs121913387
Max Magnitude0
ClinVar
Risk rs121913387(T;T)
Alt rs121913387(T;T)
Reference Rs121913387(C;C)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene CDKN2A
CLNDBN Neoplasm
Reversed 1
HGVS NC_000009.11:g.21971186G>A
CLNSRC
CLNACC RCV000430418.1,