rs17375901
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common on affy axiom data |
| Make rs17375901(C;T) |
| Make rs17375901(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 11792459 |
| Gene | MTHFR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17375901 |
| dbSNP (classic) | rs17375901 |
| ClinGen | rs17375901 |
| ebi | rs17375901 |
| HLI | rs17375901 |
| Exac | rs17375901 |
| Gnomad | rs17375901 |
| Varsome | rs17375901 |
| LitVar | rs17375901 |
| Map | rs17375901 |
| PheGenI | rs17375901 |
| Biobank | rs17375901 |
| 1000 genomes | rs17375901 |
| hgdp | rs17375901 |
| ensembl | rs17375901 |
| geneview | rs17375901 |
| scholar | rs17375901 |
| rs17375901 | |
| pharmgkb | rs17375901 |
| gwascentral | rs17375901 |
| openSNP | rs17375901 |
| 23andMe | rs17375901 |
| SNPshot | rs17375901 |
| SNPdbe | rs17375901 |
| MSV3d | rs17375901 |
| GWAS Ctlg | rs17375901 |
| GMAF | 0.02984 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | T |
| P-val | 6E-7 |
| Odds Ratio | 1.26 None |
[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)
