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rs3096299

From SNPedia

Orientationminus
Stabilizedminus
Make rs3096299(C;C)
Make rs3096299(C;T)
Make rs3096299(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position89382255
GeneANKRD11
is asnp
is mentioned by
dbSNPrs3096299
ebirs3096299
HLIrs3096299
Exacrs3096299
Varsomers3096299
Maprs3096299
PheGenIrs3096299
hapmaprs3096299
1000 genomesrs3096299
hgdprs3096299
ensemblrs3096299
gopubmedrs3096299
geneviewrs3096299
scholarrs3096299
googlers3096299
pharmgkbrs3096299
gwascentralrs3096299
openSNPrs3096299
23andMers3096299
23andMe allrs3096299
SNP Nexus

SNPshotrs3096299
SNPdbers3096299
MSV3drs3096299
GWAS Ctlgrs3096299
GMAF0.4467
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 4E-6
Odds Ratio 1.54 [1.28-1.86]