rs2074518
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2074518(A;A) |
Make rs2074518(A;G) |
Make rs2074518(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 34997363 |
Gene | LIG3 |
is a | snp |
is | mentioned by |
dbSNP | rs2074518 |
dbSNP (classic) | rs2074518 |
ClinGen | rs2074518 |
ebi | rs2074518 |
HLI | rs2074518 |
Exac | rs2074518 |
Gnomad | rs2074518 |
Varsome | rs2074518 |
LitVar | rs2074518 |
Map | rs2074518 |
PheGenI | rs2074518 |
Biobank | rs2074518 |
1000 genomes | rs2074518 |
hgdp | rs2074518 |
ensembl | rs2074518 |
geneview | rs2074518 |
scholar | rs2074518 |
rs2074518 | |
pharmgkb | rs2074518 |
gwascentral | rs2074518 |
openSNP | rs2074518 |
23andMe | rs2074518 |
SNPshot | rs2074518 |
SNPdbe | rs2074518 |
MSV3d | rs2074518 |
GWAS Ctlg | rs2074518 |
GMAF | 0.3255 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
23andMe blog Influences QT interval
GWAS snp | |
---|---|
PMID | [PMID 19305408] |
Trait | QT interval |
Title | Common variants at ten loci influence QT interval duation in the QTGEN Study |
Risk Allele | T |
P-val | 6E-12 |
Odds Ratio |