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rs2115386

From SNPedia

Orientationminus
Stabilizedminus
Make rs2115386(A;A)
Make rs2115386(A;G)
Make rs2115386(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position7196554
GeneINSR
is asnp
is mentioned by
dbSNPrs2115386
ebirs2115386
HLIrs2115386
Exacrs2115386
Varsomers2115386
Maprs2115386
PheGenIrs2115386
hapmaprs2115386
1000 genomesrs2115386
hgdprs2115386
ensemblrs2115386
gopubmedrs2115386
geneviewrs2115386
scholarrs2115386
googlers2115386
pharmgkbrs2115386
gwascentralrs2115386
openSNPrs2115386
23andMers2115386
23andMe allrs2115386
SNP Nexus

SNPshotrs2115386
SNPdbers2115386
MSV3drs2115386
GWAS Ctlgrs2115386
GMAF0.4963
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21441570OA-icon.png]
Trait
Title Genome-wide Meta-analysis for Severe Diabetic Retinopathy
Risk Allele C
P-val 0.000003
Odds Ratio 1.1200 [NR]


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