rs17570669
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs17570669(A;T) |
Make rs17570669(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 110815726 |
is a | snp |
is | mentioned by |
dbSNP | rs17570669 |
dbSNP (classic) | rs17570669 |
ClinGen | rs17570669 |
ebi | rs17570669 |
HLI | rs17570669 |
Exac | rs17570669 |
Gnomad | rs17570669 |
Varsome | rs17570669 |
LitVar | rs17570669 |
Map | rs17570669 |
PheGenI | rs17570669 |
Biobank | rs17570669 |
1000 genomes | rs17570669 |
hgdp | rs17570669 |
ensembl | rs17570669 |
geneview | rs17570669 |
scholar | rs17570669 |
rs17570669 | |
pharmgkb | rs17570669 |
gwascentral | rs17570669 |
openSNP | rs17570669 |
23andMe | rs17570669 |
SNPshot | rs17570669 |
SNPdbe | rs17570669 |
MSV3d | rs17570669 |
GWAS Ctlg | rs17570669 |
GMAF | 0.03306 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 20733104] Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25
[PMID 21760908] Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population