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rs9864370

From SNPedia

Orientationplus
Stabilizedplus
Make rs9864370(C;C)
Make rs9864370(C;T)
Make rs9864370(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position169198452
GeneMECOM
is asnp
is mentioned by
dbSNPrs9864370
ebirs9864370
HLIrs9864370
Exacrs9864370
Varsomers9864370
Maprs9864370
PheGenIrs9864370
hapmaprs9864370
1000 genomesrs9864370
hgdprs9864370
ensemblrs9864370
gopubmedrs9864370
geneviewrs9864370
scholarrs9864370
googlers9864370
pharmgkbrs9864370
gwascentralrs9864370
openSNPrs9864370
23andMers9864370
23andMe allrs9864370
SNP Nexus

SNPshotrs9864370
SNPdbers9864370
MSV3drs9864370
GWAS Ctlgrs9864370
GMAF0.07438
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 9E-6
Odds Ratio 2.04 [1.49-2.80]