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rs12659144

From SNPedia

Orientationplus
Stabilizedplus
Make rs12659144(C;C)
Make rs12659144(C;T)
Make rs12659144(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position174350517
is asnp
is mentioned by
dbSNPrs12659144
ebirs12659144
HLIrs12659144
Exacrs12659144
Varsomers12659144
Maprs12659144
PheGenIrs12659144
hapmaprs12659144
1000 genomesrs12659144
hgdprs12659144
ensemblrs12659144
gopubmedrs12659144
geneviewrs12659144
scholarrs12659144
googlers12659144
pharmgkbrs12659144
gwascentralrs12659144
openSNPrs12659144
23andMers12659144
23andMe allrs12659144
SNP Nexus

SNPshotrs12659144
SNPdbers12659144
MSV3drs12659144
GWAS Ctlgrs12659144
GMAF0.2236
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 G
P-val 3E-6
Odds Ratio 1.67 [1.35-2.07]