rs1362212
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs1362212(A;A) |
Make rs1362212(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 35265695 |
is a | snp |
is | mentioned by |
dbSNP | rs1362212 |
dbSNP (classic) | rs1362212 |
ClinGen | rs1362212 |
ebi | rs1362212 |
HLI | rs1362212 |
Exac | rs1362212 |
Gnomad | rs1362212 |
Varsome | rs1362212 |
LitVar | rs1362212 |
Map | rs1362212 |
PheGenI | rs1362212 |
Biobank | rs1362212 |
1000 genomes | rs1362212 |
hgdp | rs1362212 |
ensembl | rs1362212 |
geneview | rs1362212 |
scholar | rs1362212 |
rs1362212 | |
pharmgkb | rs1362212 |
gwascentral | rs1362212 |
openSNP | rs1362212 |
23andMe | rs1362212 |
SNPshot | rs1362212 |
SNPdbe | rs1362212 |
MSV3d | rs1362212 |
GWAS Ctlg | rs1362212 |
GMAF | 0.09871 |
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 | A |
P-val | 1E-13 |
Odds Ratio | 0.6900 [0.51-0.87] ms increase |