rs9851724
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9851724(C;C) |
Make rs9851724(C;T) |
Make rs9851724(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 38678444 |
is a | snp |
is | mentioned by |
dbSNP | rs9851724 |
dbSNP (classic) | rs9851724 |
ClinGen | rs9851724 |
ebi | rs9851724 |
HLI | rs9851724 |
Exac | rs9851724 |
Gnomad | rs9851724 |
Varsome | rs9851724 |
LitVar | rs9851724 |
Map | rs9851724 |
PheGenI | rs9851724 |
Biobank | rs9851724 |
1000 genomes | rs9851724 |
hgdp | rs9851724 |
ensembl | rs9851724 |
geneview | rs9851724 |
scholar | rs9851724 |
rs9851724 | |
pharmgkb | rs9851724 |
gwascentral | rs9851724 |
openSNP | rs9851724 |
23andMe | rs9851724 |
SNPshot | rs9851724 |
SNPdbe | rs9851724 |
MSV3d | rs9851724 |
GWAS Ctlg | rs9851724 |
GMAF | 0.2732 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21076409] |
Trait | |
Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
Risk Allele | C |
P-val | 6E-16 |
Odds Ratio | 0.6000 [NR] ms decrease |