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

rs121913384

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913384(G;T)
Make rs121913384(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971097
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913384
dbSNP (old)rs121913384
ClinGenrs121913384
ebirs121913384
HLIrs121913384
Exacrs121913384
Gnomadrs121913384
Varsomers121913384
Maprs121913384
PheGenIrs121913384
Biobankrs121913384
1000 genomesrs121913384
hgdprs121913384
ensemblrs121913384
gopubmedrs121913384
geneviewrs121913384
scholarrs121913384
googlers121913384
pharmgkbrs121913384
gwascentralrs121913384
openSNPrs121913384
23andMers121913384
23andMe allrs121913384
SNPshotrs121913384
SNPdbers121913384
MSV3drs121913384
GWAS Ctlgrs121913384
Max Magnitude0
ClinVar
Risk rs121913384(T;T)
Alt rs121913384(T;T)
Reference Rs121913384(G;G)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene CDKN2A
CLNDBN Neoplasm
Reversed 1
HGVS NC_000009.11:g.21971096C>A
CLNSRC
CLNACC RCV000436299.1,