rs10784762

Orientation

plus

Stabilized

plus

Make rs10784762(C;C)

Make rs10784762(C;T)

Make rs10784762(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

69130143

is a	snp
is	mentioned by
dbSNP	rs10784762
dbSNP (classic)	rs10784762
ClinGen	rs10784762
ebi	rs10784762
HLI	rs10784762
Exac	rs10784762
Gnomad	rs10784762
Varsome	rs10784762
LitVar	rs10784762
Map	rs10784762
PheGenI	rs10784762
Biobank	rs10784762
1000 genomes	rs10784762
hgdp	rs10784762
ensembl	rs10784762
geneview	rs10784762
scholar	rs10784762
google	rs10784762
pharmgkb	rs10784762
gwascentral	rs10784762
openSNP	rs10784762
23andMe	rs10784762
SNPshot	rs10784762
SNPdbe	rs10784762
MSV3d	rs10784762
GWAS Ctlg	rs10784762

GMAF

0.3953

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23534349]
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