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rs4462262

From SNPedia

Orientationplus
Stabilizedplus
Make rs4462262(C;C)
Make rs4462262(C;T)
Make rs4462262(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position57429418
is asnp
is mentioned by
dbSNPrs4462262
ebirs4462262
HLIrs4462262
Exacrs4462262
Varsomers4462262
Maprs4462262
PheGenIrs4462262
hapmaprs4462262
1000 genomesrs4462262
hgdprs4462262
ensemblrs4462262
gopubmedrs4462262
geneviewrs4462262
scholarrs4462262
googlers4462262
pharmgkbrs4462262
gwascentralrs4462262
openSNPrs4462262
23andMers4462262
23andMe allrs4462262
SNP Nexus

SNPshotrs4462262
SNPdbers4462262
MSV3drs4462262
GWAS Ctlgrs4462262
GMAF0.3471
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21310492]
Trait
Title Genome-wide Association Study of Diabetic Retinopathy in a Taiwanese Population
Risk Allele C
P-val 9E-8
Odds Ratio None None


[PMID 27768789] Impact of Genetic Loci Identified in Genome-Wide Association Studies on Diabetic Retinopathy in Chinese Patients With Type 2 Diabetes.