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rs13028485

From SNPedia

Orientationplus
Stabilizedplus
Make rs13028485(A;A)
Make rs13028485(A;G)
Make rs13028485(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position173640196
is asnp
is mentioned by
dbSNPrs13028485
ebirs13028485
HLIrs13028485
Exacrs13028485
Varsomers13028485
Maprs13028485
PheGenIrs13028485
hapmaprs13028485
1000 genomesrs13028485
hgdprs13028485
ensemblrs13028485
gopubmedrs13028485
geneviewrs13028485
scholarrs13028485
googlers13028485
pharmgkbrs13028485
gwascentralrs13028485
openSNPrs13028485
23andMers13028485
23andMe allrs13028485
SNP Nexus

SNPshotrs13028485
SNPdbers13028485
MSV3drs13028485
GWAS Ctlgrs13028485
GMAF0.1116
Max Magnitude
? (A;A) (A;G) (G;G) 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 2.17 [1.57-2.99]