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rs6800901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) multiple myeloma risk ?
(T;T) 1.1 1.3x multiple myeloma risk


Make rs6800901(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position121435346
GenePOLQ
is asnp
is mentioned by
dbSNPrs6800901
ebirs6800901
HLIrs6800901
Exacrs6800901
Varsomers6800901
Maprs6800901
PheGenIrs6800901
hapmaprs6800901
1000 genomesrs6800901
hgdprs6800901
ensemblrs6800901
gopubmedrs6800901
geneviewrs6800901
scholarrs6800901
googlers6800901
pharmgkbrs6800901
gwascentralrs6800901
openSNPrs6800901
23andMers6800901
23andMe allrs6800901
SNP Nexus

SNPshotrs6800901
SNPdbers6800901
MSV3drs6800901
GWAS Ctlgrs6800901
GMAF0.2084
Max Magnitude1.1
? (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 A
P-val 2E-6
Odds Ratio 1.31 [1.17-1.47]