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rs8099213

From SNPedia

Orientationplus
Stabilizedplus
Make rs8099213(C;C)
Make rs8099213(C;T)
Make rs8099213(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position67284976
is asnp
is mentioned by
dbSNPrs8099213
ebirs8099213
HLIrs8099213
Exacrs8099213
Varsomers8099213
Maprs8099213
PheGenIrs8099213
hapmaprs8099213
1000 genomesrs8099213
hgdprs8099213
ensemblrs8099213
gopubmedrs8099213
geneviewrs8099213
scholarrs8099213
googlers8099213
pharmgkbrs8099213
gwascentralrs8099213
openSNPrs8099213
23andMers8099213
23andMe allrs8099213
SNP Nexus

SNPshotrs8099213
SNPdbers8099213
MSV3drs8099213
GWAS Ctlgrs8099213
GMAF0.494
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 A
P-val 5E-6
Odds Ratio 1.52 [1.27-1.81]