rs6861497
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6861497(A;A) |
Make rs6861497(A;G) |
Make rs6861497(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 102067882 |
is a | snp |
is | mentioned by |
dbSNP | rs6861497 |
dbSNP (classic) | rs6861497 |
ClinGen | rs6861497 |
ebi | rs6861497 |
HLI | rs6861497 |
Exac | rs6861497 |
Gnomad | rs6861497 |
Varsome | rs6861497 |
LitVar | rs6861497 |
Map | rs6861497 |
PheGenI | rs6861497 |
Biobank | rs6861497 |
1000 genomes | rs6861497 |
hgdp | rs6861497 |
ensembl | rs6861497 |
geneview | rs6861497 |
scholar | rs6861497 |
rs6861497 | |
pharmgkb | rs6861497 |
gwascentral | rs6861497 |
openSNP | rs6861497 |
23andMe | rs6861497 |
SNPshot | rs6861497 |
SNPdbe | rs6861497 |
MSV3d | rs6861497 |
GWAS Ctlg | rs6861497 |
GMAF | 0.4045 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23534349] |
Trait | QRS duration |
Title | Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans. |
Risk Allele | A |
P-val | 5E-6 |
Odds Ratio | 2.34 [NR] ms increase |