rs17042171
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs17042171(A;A) |
| Make rs17042171(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 110787131 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17042171 |
| dbSNP (classic) | rs17042171 |
| ClinGen | rs17042171 |
| ebi | rs17042171 |
| HLI | rs17042171 |
| Exac | rs17042171 |
| Gnomad | rs17042171 |
| Varsome | rs17042171 |
| LitVar | rs17042171 |
| Map | rs17042171 |
| PheGenI | rs17042171 |
| Biobank | rs17042171 |
| 1000 genomes | rs17042171 |
| hgdp | rs17042171 |
| ensembl | rs17042171 |
| geneview | rs17042171 |
| scholar | rs17042171 |
| rs17042171 | |
| pharmgkb | rs17042171 |
| gwascentral | rs17042171 |
| openSNP | rs17042171 |
| 23andMe | rs17042171 |
| SNPshot | rs17042171 |
| SNPdbe | rs17042171 |
| MSV3d | rs17042171 |
| GWAS Ctlg | rs17042171 |
| GMAF | 0.2759 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19597492 ]
|
| Trait | Atrial fibrillation |
| Title | Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry |
| Risk Allele | A |
| P-val | 4E-63 |
| Odds Ratio | 1.65 None |
[PMID 26467376] Association of rs17042171 with chromosome 4q25 with atrial fibrillation in Chinese Han populations
[PMID 26497660] Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF)
[PMID 30110000] [Rs17042171 at chromosome 4q25 is associated with atrial fibrillation in the Chinese Han population from the central plains].
