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rs10784762

From SNPedia

Orientationplus
Stabilizedplus
Make rs10784762(C;C)
Make rs10784762(C;T)
Make rs10784762(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position69130143
is asnp
is mentioned by
dbSNPrs10784762
ebirs10784762
HLIrs10784762
Exacrs10784762
Varsomers10784762
Maprs10784762
PheGenIrs10784762
hapmaprs10784762
1000 genomesrs10784762
hgdprs10784762
ensemblrs10784762
gopubmedrs10784762
geneviewrs10784762
scholarrs10784762
googlers10784762
pharmgkbrs10784762
gwascentralrs10784762
openSNPrs10784762
23andMers10784762
23andMe allrs10784762
SNP Nexus

SNPshotrs10784762
SNPdbers10784762
MSV3drs10784762
GWAS Ctlgrs10784762
GMAF0.3953
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23534349OA-icon.png]
Trait QRS duration
Title Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
Risk Allele T
P-val 6E-6
Odds Ratio 2.38 [NR] ms decrease