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rs7577599

From SNPedia

Orientationplus
Stabilizedplus
Make rs7577599(C;C)
Make rs7577599(C;T)
Make rs7577599(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position25390277
GeneDTNB
is asnp
is mentioned by
dbSNPrs7577599
ebirs7577599
HLIrs7577599
Exacrs7577599
Varsomers7577599
Maprs7577599
PheGenIrs7577599
hapmaprs7577599
1000 genomesrs7577599
hgdprs7577599
ensemblrs7577599
gopubmedrs7577599
geneviewrs7577599
scholarrs7577599
googlers7577599
pharmgkbrs7577599
gwascentralrs7577599
openSNPrs7577599
23andMers7577599
23andMe allrs7577599
SNP Nexus

SNPshotrs7577599
SNPdbers7577599
MSV3drs7577599
GWAS Ctlgrs7577599
GMAF0.3613
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 6E-6
Odds Ratio 1.43 [1.22-1.67]