rs1524976
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1524976(A;A) |
Make rs1524976(A;G) |
Make rs1524976(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 65500713 |
Gene | MAGI1 |
is a | snp |
is | mentioned by |
dbSNP | rs1524976 |
dbSNP (classic) | rs1524976 |
ClinGen | rs1524976 |
ebi | rs1524976 |
HLI | rs1524976 |
Exac | rs1524976 |
Gnomad | rs1524976 |
Varsome | rs1524976 |
LitVar | rs1524976 |
Map | rs1524976 |
PheGenI | rs1524976 |
Biobank | rs1524976 |
1000 genomes | rs1524976 |
hgdp | rs1524976 |
ensembl | rs1524976 |
geneview | rs1524976 |
scholar | rs1524976 |
rs1524976 | |
pharmgkb | rs1524976 |
gwascentral | rs1524976 |
openSNP | rs1524976 |
23andMe | rs1524976 |
SNPshot | rs1524976 |
SNPdbe | rs1524976 |
MSV3d | rs1524976 |
GWAS Ctlg | rs1524976 |
GMAF | 0.1157 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23534349] |
Trait | PR interval |
Title | Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans. |
Risk Allele | A |
P-val | 8E-6 |
Odds Ratio | 8.00 [NR] ms increase |