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rs12638862

From SNPedia

Orientationplus
Stabilizedplus
Make rs12638862(A;A)
Make rs12638862(A;G)
Make rs12638862(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position169759718
is asnp
is mentioned by
dbSNPrs12638862
ClinGenrs12638862
ebirs12638862
HLIrs12638862
Exacrs12638862
Varsomers12638862
Maprs12638862
PheGenIrs12638862
hapmaprs12638862
1000 genomesrs12638862
hgdprs12638862
ensemblrs12638862
gopubmedrs12638862
geneviewrs12638862
scholarrs12638862
googlers12638862
pharmgkbrs12638862
gwascentralrs12638862
openSNPrs12638862
23andMers12638862
23andMe allrs12638862
SNP Nexus

SNPshotrs12638862
SNPdbers12638862
MSV3drs12638862
GWAS Ctlgrs12638862
GMAF0.3306
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23502783]
Trait Multiple myeloma (IgH translocation)
Title The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Risk Allele A
P-val 2E-6
Odds Ratio 1.37 [1.20-1.56]