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rs4521323

From SNPedia

Orientationplus
Stabilizedplus
Make rs4521323(A;A)
Make rs4521323(A;C)
Make rs4521323(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position173734763
GeneLOC101928478
is asnp
is mentioned by
dbSNPrs4521323
ebirs4521323
HLIrs4521323
Exacrs4521323
Varsomers4521323
Maprs4521323
PheGenIrs4521323
hapmaprs4521323
1000 genomesrs4521323
hgdprs4521323
ensemblrs4521323
gopubmedrs4521323
geneviewrs4521323
scholarrs4521323
googlers4521323
pharmgkbrs4521323
gwascentralrs4521323
openSNPrs4521323
23andMers4521323
23andMe allrs4521323
SNP Nexus

SNPshotrs4521323
SNPdbers4521323
MSV3drs4521323
GWAS Ctlgrs4521323
GMAF0.4275
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 9E-6
Odds Ratio 1.28 [1.15-1.43]