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rs9866141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9866141(C;T)
Make rs9866141(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position157232790
GeneLOC101928236
is asnp
is mentioned by
dbSNPrs9866141
ebirs9866141
HLIrs9866141
Exacrs9866141
Varsomers9866141
Maprs9866141
PheGenIrs9866141
hapmaprs9866141
1000 genomesrs9866141
hgdprs9866141
ensemblrs9866141
gopubmedrs9866141
geneviewrs9866141
scholarrs9866141
googlers9866141
pharmgkbrs9866141
gwascentralrs9866141
openSNPrs9866141
23andMers9866141
23andMe allrs9866141
SNP Nexus

SNPshotrs9866141
SNPdbers9866141
MSV3drs9866141
GWAS Ctlgrs9866141
GMAF0.06152
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21441570OA-icon.png]
Trait
Title Genome-wide Meta-analysis for Severe Diabetic Retinopathy
Risk Allele T
P-val 9E-7
Odds Ratio 1.0200 [NR]