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

rs398123152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123152(-;-)
Make rs398123152(-;G)
Make rs398123152(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position21974721
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs398123152
ebirs398123152
HLIrs398123152
Exacrs398123152
Varsomers398123152
Maprs398123152
PheGenIrs398123152
hapmaprs398123152
1000 genomesrs398123152
hgdprs398123152
ensemblrs398123152
gopubmedrs398123152
geneviewrs398123152
scholarrs398123152
googlers398123152
pharmgkbrs398123152
gwascentralrs398123152
openSNPrs398123152
23andMers398123152
23andMe allrs398123152
SNP Nexus

SNPshotrs398123152
SNPdbers398123152
MSV3drs398123152
GWAS Ctlgrs398123152
Max Magnitude0
ClinVar
Risk rs398123152(G;G)
Alt rs398123152(G;G)
Reference rs398123152(;)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome Cutaneous malignant melanoma 1
Variation info
Gene CDKN2A
CLNDBN not provided Hereditary cancer-predisposing syndrome Cutaneous malignant melanoma 1
Reversed 1
HGVS NC_000009.11:g.21974721dupC
CLNSRC ClinVar
CLNACC RCV000078113.3, RCV000166566.1, RCV000173061.1,