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rs10026364

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10026364(C;T)
Make rs10026364(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position134601585
is asnp
is mentioned by
dbSNPrs10026364
ebirs10026364
HLIrs10026364
Exacrs10026364
Varsomers10026364
Maprs10026364
PheGenIrs10026364
hapmaprs10026364
1000 genomesrs10026364
hgdprs10026364
ensemblrs10026364
gopubmedrs10026364
geneviewrs10026364
scholarrs10026364
googlers10026364
pharmgkbrs10026364
gwascentralrs10026364
openSNPrs10026364
23andMers10026364
23andMe allrs10026364
SNP Nexus

SNPshotrs10026364
SNPdbers10026364
MSV3drs10026364
GWAS Ctlgrs10026364
GMAF0.0528
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21347282OA-icon.png]
Trait
Title Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele T
P-val 0.000004
Odds Ratio 1.2800 [1.15-1.42]