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rs17112190

From SNPedia

Orientationplus
Stabilizedplus
Make rs17112190(A;A)
Make rs17112190(A;G)
Make rs17112190(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position96880089
GeneLCOR
is asnp
is mentioned by
dbSNPrs17112190
ebirs17112190
HLIrs17112190
Exacrs17112190
Varsomers17112190
Maprs17112190
PheGenIrs17112190
hapmaprs17112190
1000 genomesrs17112190
hgdprs17112190
ensemblrs17112190
gopubmedrs17112190
geneviewrs17112190
scholarrs17112190
googlers17112190
pharmgkbrs17112190
gwascentralrs17112190
openSNPrs17112190
23andMers17112190
23andMe allrs17112190
SNP Nexus

SNPshotrs17112190
SNPdbers17112190
MSV3drs17112190
GWAS Ctlgrs17112190
GMAF0.118
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 9E-7
Odds Ratio 1.80 [1.42-2.27]