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rs7769051

From SNPedia

Orientationplus
Stabilizedplus
Make rs7769051(A;A)
Make rs7769051(A;C)
Make rs7769051(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position132825657
is asnp
is mentioned by
dbSNPrs7769051
ebirs7769051
HLIrs7769051
Exacrs7769051
Varsomers7769051
Maprs7769051
PheGenIrs7769051
hapmaprs7769051
1000 genomesrs7769051
hgdprs7769051
ensemblrs7769051
gopubmedrs7769051
geneviewrs7769051
scholarrs7769051
googlers7769051
pharmgkbrs7769051
gwascentralrs7769051
openSNPrs7769051
23andMers7769051
23andMe allrs7769051
SNP Nexus

SNPshotrs7769051
SNPdbers7769051
MSV3drs7769051
GWAS Ctlgrs7769051
GMAF0.174
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21150874OA-icon.png]
Trait
Title A genome-wide association study for diabetic nephropathy genes in African Americans
Risk Allele A
P-val 0.000002
Odds Ratio 1.2800 [1.16-1.42]