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rs2055729

From SNPedia

Orientationplus
Stabilizedplus
Make rs2055729(A;A)
Make rs2055729(A;G)
Make rs2055729(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position9935152
is asnp
is mentioned by
dbSNPrs2055729
ebirs2055729
HLIrs2055729
Exacrs2055729
Varsomers2055729
Maprs2055729
PheGenIrs2055729
hapmaprs2055729
1000 genomesrs2055729
hgdprs2055729
ensemblrs2055729
gopubmedrs2055729
geneviewrs2055729
scholarrs2055729
googlers2055729
pharmgkbrs2055729
gwascentralrs2055729
openSNPrs2055729
23andMers2055729
23andMe allrs2055729
SNP Nexus

SNPshotrs2055729
SNPdbers2055729
MSV3drs2055729
GWAS Ctlgrs2055729
GMAF0.489
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23502783]
Trait Multiple myeloma (hyperdiploidy)
Title The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Risk Allele G
P-val 8E-7
Odds Ratio 1.30 [1.17-1.45]