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rs5763911

From SNPedia

Orientationplus
Stabilizedplus
Make rs5763911(C;C)
Make rs5763911(C;T)
Make rs5763911(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position20443002
GeneKLHL22
is asnp
is mentioned by
dbSNPrs5763911
ebirs5763911
HLIrs5763911
Exacrs5763911
Varsomers5763911
Maprs5763911
PheGenIrs5763911
hapmaprs5763911
1000 genomesrs5763911
hgdprs5763911
ensemblrs5763911
gopubmedrs5763911
geneviewrs5763911
scholarrs5763911
googlers5763911
pharmgkbrs5763911
gwascentralrs5763911
openSNPrs5763911
23andMers5763911
23andMe allrs5763911
SNP Nexus

SNPshotrs5763911
SNPdbers5763911
MSV3drs5763911
GWAS Ctlgrs5763911
GMAF0.05051
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 6E-6
Odds Ratio .52 [0.3-0.74] unit decrease