rs1733724
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1733724(C;C) |
Make rs1733724(C;T) |
Make rs1733724(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 52464217 |
Gene | LINC01468 |
is a | snp |
is | mentioned by |
dbSNP | rs1733724 |
dbSNP (classic) | rs1733724 |
ClinGen | rs1733724 |
ebi | rs1733724 |
HLI | rs1733724 |
Exac | rs1733724 |
Gnomad | rs1733724 |
Varsome | rs1733724 |
LitVar | rs1733724 |
Map | rs1733724 |
PheGenI | rs1733724 |
Biobank | rs1733724 |
1000 genomes | rs1733724 |
hgdp | rs1733724 |
ensembl | rs1733724 |
geneview | rs1733724 |
scholar | rs1733724 |
rs1733724 | |
pharmgkb | rs1733724 |
gwascentral | rs1733724 |
openSNP | rs1733724 |
23andMe | rs1733724 |
SNPshot | rs1733724 |
SNPdbe | rs1733724 |
MSV3d | rs1733724 |
GWAS Ctlg | rs1733724 |
GMAF | 0.141 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20062063] |
Trait | Electrocardiographic traits |
Title | Several common variants modulate heart rate, PR interval and QRS duration |
Risk Allele | T |
P-val | 7E-8 |
Odds Ratio | 5.62 [3.58-7.66] % SD increase |
GWAS snp | |
---|---|
PMID | [PMID 21076409] |
Trait | |
Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
Risk Allele | A |
P-val | 3E-8 |
Odds Ratio | 0.4900 [0.31-0.67] ms increase |