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rs9918807

From SNPedia

Orientationplus
Stabilizedplus
Make rs9918807(C;C)
Make rs9918807(C;T)
Make rs9918807(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position129664393
is asnp
is mentioned by
dbSNPrs9918807
ebirs9918807
HLIrs9918807
Exacrs9918807
Varsomers9918807
Maprs9918807
PheGenIrs9918807
hapmaprs9918807
1000 genomesrs9918807
hgdprs9918807
ensemblrs9918807
gopubmedrs9918807
geneviewrs9918807
scholarrs9918807
googlers9918807
pharmgkbrs9918807
gwascentralrs9918807
openSNPrs9918807
23andMers9918807
23andMe allrs9918807
SNP Nexus

SNPshotrs9918807
SNPdbers9918807
MSV3drs9918807
GWAS Ctlgrs9918807
GMAF0.09871
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23393555OA-icon.png]
Trait Retinopathy in non-diabetics
Title Genome-wide association study of retinopathy in individuals without diabetes.
Risk Allele T
P-val 5E-6
Odds Ratio .47 [0.27-0.67] unit decrease