rs12210810
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs12210810(C;C) |
Make rs12210810(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 118332041 |
is a | snp |
is | mentioned by |
dbSNP | rs12210810 |
dbSNP (classic) | rs12210810 |
ClinGen | rs12210810 |
ebi | rs12210810 |
HLI | rs12210810 |
Exac | rs12210810 |
Gnomad | rs12210810 |
Varsome | rs12210810 |
LitVar | rs12210810 |
Map | rs12210810 |
PheGenI | rs12210810 |
Biobank | rs12210810 |
1000 genomes | rs12210810 |
hgdp | rs12210810 |
ensembl | rs12210810 |
geneview | rs12210810 |
scholar | rs12210810 |
rs12210810 | |
pharmgkb | rs12210810 |
gwascentral | rs12210810 |
openSNP | rs12210810 |
23andMe | rs12210810 |
SNPshot | rs12210810 |
SNPdbe | rs12210810 |
MSV3d | rs12210810 |
GWAS Ctlg | rs12210810 |
GMAF | 0.02204 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19305409![]() |
Trait | QT interval |
Title | Common variants at ten loci modulate the QT interval duration in the QTSCD Study |
Risk Allele | C |
P-val | 2E-17 |
Odds Ratio | 3.13 [2.29-3.97] ms decrease |