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rs4737547

From SNPedia

Orientationplus
Stabilizedplus
Make rs4737547(A;A)
Make rs4737547(A;G)
Make rs4737547(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position59633105
is asnp
is mentioned by
dbSNPrs4737547
ebirs4737547
HLIrs4737547
Exacrs4737547
Varsomers4737547
Maprs4737547
PheGenIrs4737547
hapmaprs4737547
1000 genomesrs4737547
hgdprs4737547
ensemblrs4737547
gopubmedrs4737547
geneviewrs4737547
scholarrs4737547
googlers4737547
pharmgkbrs4737547
gwascentralrs4737547
openSNPrs4737547
23andMers4737547
23andMe allrs4737547
SNP Nexus

SNPshotrs4737547
SNPdbers4737547
MSV3drs4737547
GWAS Ctlgrs4737547
GMAF0.4541
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 G
P-val 3E-6
Odds Ratio 1.30 [1.17-1.45]