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rs6746082

From SNPedia

Orientationplus
Stabilizedplus
Make rs6746082(A;A)
Make rs6746082(A;C)
Make rs6746082(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position25436375
GeneDTNB
is asnp
is mentioned by
dbSNPrs6746082
ebirs6746082
HLIrs6746082
Exacrs6746082
Varsomers6746082
Maprs6746082
PheGenIrs6746082
hapmaprs6746082
1000 genomesrs6746082
hgdprs6746082
ensemblrs6746082
gopubmedrs6746082
geneviewrs6746082
scholarrs6746082
googlers6746082
pharmgkbrs6746082
gwascentralrs6746082
openSNPrs6746082
23andMers6746082
23andMe allrs6746082
SNP Nexus

SNPshotrs6746082
SNPdbers6746082
MSV3drs6746082
GWAS Ctlgrs6746082
GMAF0.405
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22120009]
Trait
Title Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
Risk Allele A
P-val 4E-7
Odds Ratio 1.2900 None


[PMID 24449210] Inherited genetic susceptibility to monoclonal gammopathy of unknown significance