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rs11867934

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11867934(C;T)
Make rs11867934(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position17030090
is asnp
is mentioned by
dbSNPrs11867934
ebirs11867934
HLIrs11867934
Exacrs11867934
Varsomers11867934
Maprs11867934
PheGenIrs11867934
hapmaprs11867934
1000 genomesrs11867934
hgdprs11867934
ensemblrs11867934
gopubmedrs11867934
geneviewrs11867934
scholarrs11867934
googlers11867934
pharmgkbrs11867934
gwascentralrs11867934
openSNPrs11867934
23andMers11867934
23andMe allrs11867934
SNP Nexus

SNPshotrs11867934
SNPdbers11867934
MSV3drs11867934
GWAS Ctlgrs11867934
GMAF0.18
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 C
P-val 0.000007
Odds Ratio 1.4300 [NR]