rs2579330
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2579330(A;A) |
| Make rs2579330(A;G) |
| Make rs2579330(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 71261172 |
| Gene | SLC4A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2579330 |
| dbSNP (classic) | rs2579330 |
| ClinGen | rs2579330 |
| ebi | rs2579330 |
| HLI | rs2579330 |
| Exac | rs2579330 |
| Gnomad | rs2579330 |
| Varsome | rs2579330 |
| LitVar | rs2579330 |
| Map | rs2579330 |
| PheGenI | rs2579330 |
| Biobank | rs2579330 |
| 1000 genomes | rs2579330 |
| hgdp | rs2579330 |
| ensembl | rs2579330 |
| geneview | rs2579330 |
| scholar | rs2579330 |
| rs2579330 | |
| pharmgkb | rs2579330 |
| gwascentral | rs2579330 |
| openSNP | rs2579330 |
| 23andMe | rs2579330 |
| SNPshot | rs2579330 |
| SNPdbe | rs2579330 |
| MSV3d | rs2579330 |
| GWAS Ctlg | rs2579330 |
| GMAF | 0.1033 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23166209 ]
|
| Trait | QT interval |
| Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
| Risk Allele | C |
| P-val | 1E-6 |
| Odds Ratio | 1.36 [0.81-1.91] unit increase |
