rs2708240
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2708240(A;A) |
Make rs2708240(A;G) |
Make rs2708240(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 147880445 |
Gene | CNTNAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs2708240 |
dbSNP (classic) | rs2708240 |
ClinGen | rs2708240 |
ebi | rs2708240 |
HLI | rs2708240 |
Exac | rs2708240 |
Gnomad | rs2708240 |
Varsome | rs2708240 |
LitVar | rs2708240 |
Map | rs2708240 |
PheGenI | rs2708240 |
Biobank | rs2708240 |
1000 genomes | rs2708240 |
hgdp | rs2708240 |
ensembl | rs2708240 |
geneview | rs2708240 |
scholar | rs2708240 |
rs2708240 | |
pharmgkb | rs2708240 |
gwascentral | rs2708240 |
openSNP | rs2708240 |
23andMe | rs2708240 |
SNPshot | rs2708240 |
SNPdbe | rs2708240 |
MSV3d | rs2708240 |
GWAS Ctlg | rs2708240 |
GMAF | 0.3999 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23459443] |
Trait | QT interval (interaction) |
Title | Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. |
Risk Allele | A |
P-val | 4E-6 |
Odds Ratio | NR NR |