Rs10509328

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Orientationplus
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ReferenceGRCh37.p10 37.5/138
Chromosome10
Position72767409
is asnp
is mentioned by
dbSNPrs10509328
Exacrs10509328
PheGenIrs10509328
nextbiors10509328
hapmaprs10509328
1000 genomesrs10509328
hgdprs10509328
ensemblrs10509328
gopubmedrs10509328
geneviewrs10509328
scholarrs10509328
googlers10509328
pharmgkbrs10509328
gwascentralrs10509328
openSNPrs10509328
23andMers10509328
23andMe allrs10509328
SNP Nexus

SNPshotrs10509328
SNPdbers10509328
MSV3drs10509328
GMAF0.1157
Max Magnitude
? (C;C) (C;T) (T;T) 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 1E-6
Odds Ratio 1.86 [1.45-2.39]