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rs10180663

From SNPedia

Orientationplus
Stabilizedplus
Make rs10180663(C;C)
Make rs10180663(C;T)
Make rs10180663(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position25410373
GeneDTNB
is asnp
is mentioned by
dbSNPrs10180663
ebirs10180663
HLIrs10180663
Exacrs10180663
Varsomers10180663
Maprs10180663
PheGenIrs10180663
hapmaprs10180663
1000 genomesrs10180663
hgdprs10180663
ensemblrs10180663
gopubmedrs10180663
geneviewrs10180663
scholarrs10180663
googlers10180663
pharmgkbrs10180663
gwascentralrs10180663
openSNPrs10180663
23andMers10180663
23andMe allrs10180663
SNP Nexus

SNPshotrs10180663
SNPdbers10180663
MSV3drs10180663
GWAS Ctlgrs10180663
GMAF0.472
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 A
P-val 2E-6
Odds Ratio 1.64 [1.34-2.02]