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rs6601327

From SNPedia

Orientationplus
Stabilizedplus
Make rs6601327(A;A)
Make rs6601327(A;G)
Make rs6601327(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position9538022
is asnp
is mentioned by
dbSNPrs6601327
ebirs6601327
HLIrs6601327
Exacrs6601327
Varsomers6601327
Maprs6601327
PheGenIrs6601327
hapmaprs6601327
1000 genomesrs6601327
hgdprs6601327
ensemblrs6601327
gopubmedrs6601327
geneviewrs6601327
scholarrs6601327
googlers6601327
pharmgkbrs6601327
gwascentralrs6601327
openSNPrs6601327
23andMers6601327
23andMe allrs6601327
SNP Nexus

SNPshotrs6601327
SNPdbers6601327
MSV3drs6601327
GWAS Ctlgrs6601327
GMAF0.4885
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-6
Odds Ratio 1.27 [1.14-1.41]