Have questions? Visit https://www.reddit.com/r/SNPedia

rs7086888

From SNPedia

Orientationplus
Stabilizedplus
Make rs7086888(A;A)
Make rs7086888(A;G)
Make rs7086888(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position4634004
is asnp
is mentioned by
dbSNPrs7086888
ebirs7086888
HLIrs7086888
Exacrs7086888
Varsomers7086888
Maprs7086888
PheGenIrs7086888
hapmaprs7086888
1000 genomesrs7086888
hgdprs7086888
ensemblrs7086888
gopubmedrs7086888
geneviewrs7086888
scholarrs7086888
googlers7086888
pharmgkbrs7086888
gwascentralrs7086888
openSNPrs7086888
23andMers7086888
23andMe allrs7086888
SNP Nexus

SNPshotrs7086888
SNPdbers7086888
MSV3drs7086888
GWAS Ctlgrs7086888
GMAF0.1047
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 G
P-val 8E-6
Odds Ratio 1.87 [1.42-2.46]