rs11663697
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs11663697(G;T) |
Make rs11663697(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 77023179 |
Gene | MBP |
is a | snp |
is | mentioned by |
dbSNP | rs11663697 |
dbSNP (classic) | rs11663697 |
ClinGen | rs11663697 |
ebi | rs11663697 |
HLI | rs11663697 |
Exac | rs11663697 |
Gnomad | rs11663697 |
Varsome | rs11663697 |
LitVar | rs11663697 |
Map | rs11663697 |
PheGenI | rs11663697 |
Biobank | rs11663697 |
1000 genomes | rs11663697 |
hgdp | rs11663697 |
ensembl | rs11663697 |
geneview | rs11663697 |
scholar | rs11663697 |
rs11663697 | |
pharmgkb | rs11663697 |
gwascentral | rs11663697 |
openSNP | rs11663697 |
23andMe | rs11663697 |
SNPshot | rs11663697 |
SNPdbe | rs11663697 |
MSV3d | rs11663697 |
GWAS Ctlg | rs11663697 |
GMAF | 0.01102 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23166209] |
Trait | QT interval |
Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
Risk Allele | G |
P-val | 9E-6 |
Odds Ratio | 13.71 [7.75-19.67] unit decrease |