rs1886512
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1886512(A;A) |
Make rs1886512(A;T) |
Make rs1886512(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 73946049 |
Gene | KLF12 |
is a | snp |
is | mentioned by |
dbSNP | rs1886512 |
dbSNP (classic) | rs1886512 |
ClinGen | rs1886512 |
ebi | rs1886512 |
HLI | rs1886512 |
Exac | rs1886512 |
Gnomad | rs1886512 |
Varsome | rs1886512 |
LitVar | rs1886512 |
Map | rs1886512 |
PheGenI | rs1886512 |
Biobank | rs1886512 |
1000 genomes | rs1886512 |
hgdp | rs1886512 |
ensembl | rs1886512 |
geneview | rs1886512 |
scholar | rs1886512 |
rs1886512 | |
pharmgkb | rs1886512 |
gwascentral | rs1886512 |
openSNP | rs1886512 |
23andMe | rs1886512 |
SNPshot | rs1886512 |
SNPdbe | rs1886512 |
MSV3d | rs1886512 |
GWAS Ctlg | rs1886512 |
GMAF | 0.3567 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 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-8 |
Odds Ratio | 0.4000 [0.26-0.54] ms decrease |