rs13375391
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13375391(A;A) |
Make rs13375391(A;G) |
Make rs13375391(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 185825751 |
Gene | HMCN1 |
is a | snp |
is | mentioned by |
dbSNP | rs13375391 |
dbSNP (classic) | rs13375391 |
ClinGen | rs13375391 |
ebi | rs13375391 |
HLI | rs13375391 |
Exac | rs13375391 |
Gnomad | rs13375391 |
Varsome | rs13375391 |
LitVar | rs13375391 |
Map | rs13375391 |
PheGenI | rs13375391 |
Biobank | rs13375391 |
1000 genomes | rs13375391 |
hgdp | rs13375391 |
ensembl | rs13375391 |
geneview | rs13375391 |
scholar | rs13375391 |
rs13375391 | |
pharmgkb | rs13375391 |
gwascentral | rs13375391 |
openSNP | rs13375391 |
23andMe | rs13375391 |
SNPshot | rs13375391 |
SNPdbe | rs13375391 |
MSV3d | rs13375391 |
GWAS Ctlg | rs13375391 |
GMAF | 0.01699 |
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 | 9E-6 |
Odds Ratio | 5.82 [NR] ms increase |