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rs11157317

From SNPedia

Orientationplus
Stabilizedplus
Make rs11157317(C;C)
Make rs11157317(C;T)
Make rs11157317(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position42934256
is asnp
is mentioned by
dbSNPrs11157317
ebirs11157317
HLIrs11157317
Exacrs11157317
Varsomers11157317
Maprs11157317
PheGenIrs11157317
hapmaprs11157317
1000 genomesrs11157317
hgdprs11157317
ensemblrs11157317
gopubmedrs11157317
geneviewrs11157317
scholarrs11157317
googlers11157317
pharmgkbrs11157317
gwascentralrs11157317
openSNPrs11157317
23andMers11157317
23andMe allrs11157317
SNP Nexus

SNPshotrs11157317
SNPdbers11157317
MSV3drs11157317
GWAS Ctlgrs11157317
GMAF0.2897
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 1.29 [1.15-1.44]