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rs11026318

From SNPedia

Orientationplus
Stabilizedplus
Make rs11026318(C;C)
Make rs11026318(C;T)
Make rs11026318(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position21875334
is asnp
is mentioned by
dbSNPrs11026318
ebirs11026318
HLIrs11026318
Exacrs11026318
Varsomers11026318
Maprs11026318
PheGenIrs11026318
hapmaprs11026318
1000 genomesrs11026318
hgdprs11026318
ensemblrs11026318
gopubmedrs11026318
geneviewrs11026318
scholarrs11026318
googlers11026318
pharmgkbrs11026318
gwascentralrs11026318
openSNPrs11026318
23andMers11026318
23andMe allrs11026318
SNP Nexus

SNPshotrs11026318
SNPdbers11026318
MSV3drs11026318
GWAS Ctlgrs11026318
GMAF0.1993
Max Magnitude
? (C;C) (C;T) (T;T) 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 A
P-val 9E-6
Odds Ratio 2.33 [1.60-3.38]