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rs10004839

From SNPedia

Orientationplus
Stabilizedplus
Make rs10004839(C;C)
Make rs10004839(C;T)
Make rs10004839(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position137233658
is asnp
is mentioned by
dbSNPrs10004839
ClinGenrs10004839
ebirs10004839
HLIrs10004839
Exacrs10004839
Varsomers10004839
Maprs10004839
PheGenIrs10004839
hapmaprs10004839
1000 genomesrs10004839
hgdprs10004839
ensemblrs10004839
gopubmedrs10004839
geneviewrs10004839
scholarrs10004839
googlers10004839
pharmgkbrs10004839
gwascentralrs10004839
openSNPrs10004839
23andMers10004839
23andMe allrs10004839
SNP Nexus

SNPshotrs10004839
SNPdbers10004839
MSV3drs10004839
GWAS Ctlgrs10004839
GMAF0.04132
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 5E-6
Odds Ratio .57 [0.32-0.82] unit increase