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rs7144018

From SNPedia

Orientationplus
Stabilizedplus
Make rs7144018(C;C)
Make rs7144018(C;T)
Make rs7144018(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position57140349
is asnp
is mentioned by
dbSNPrs7144018
ebirs7144018
HLIrs7144018
Exacrs7144018
Varsomers7144018
Maprs7144018
PheGenIrs7144018
hapmaprs7144018
1000 genomesrs7144018
hgdprs7144018
ensemblrs7144018
gopubmedrs7144018
geneviewrs7144018
scholarrs7144018
googlers7144018
pharmgkbrs7144018
gwascentralrs7144018
openSNPrs7144018
23andMers7144018
23andMe allrs7144018
SNP Nexus

SNPshotrs7144018
SNPdbers7144018
MSV3drs7144018
GWAS Ctlgrs7144018
GMAF0.258
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 9E-6
Odds Ratio 1.85 [1.41-2.44]