rs991014
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs991014(A;A) |
Make rs991014(A;G) |
Make rs991014(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 44859921 |
Gene | SETBP1 |
is a | snp |
is | mentioned by |
dbSNP | rs991014 |
dbSNP (classic) | rs991014 |
ClinGen | rs991014 |
ebi | rs991014 |
HLI | rs991014 |
Exac | rs991014 |
Gnomad | rs991014 |
Varsome | rs991014 |
LitVar | rs991014 |
Map | rs991014 |
PheGenI | rs991014 |
Biobank | rs991014 |
1000 genomes | rs991014 |
hgdp | rs991014 |
ensembl | rs991014 |
geneview | rs991014 |
scholar | rs991014 |
rs991014 | |
pharmgkb | rs991014 |
gwascentral | rs991014 |
openSNP | rs991014 |
23andMe | rs991014 |
SNPshot | rs991014 |
SNPdbe | rs991014 |
MSV3d | rs991014 |
GWAS Ctlg | rs991014 |
GMAF | 0.3297 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21076409] |
Trait | |
Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
Risk Allele | T |
P-val | 6E-10 |
Odds Ratio | 0.4200 [0.28-0.56] ms increase |