rs29784
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs29784(A;A) |
| Make rs29784(A;G) |
| Make rs29784(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 173168305 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs29784 |
| dbSNP (classic) | rs29784 |
| ClinGen | rs29784 |
| ebi | rs29784 |
| HLI | rs29784 |
| Exac | rs29784 |
| Gnomad | rs29784 |
| Varsome | rs29784 |
| LitVar | rs29784 |
| Map | rs29784 |
| PheGenI | rs29784 |
| Biobank | rs29784 |
| 1000 genomes | rs29784 |
| hgdp | rs29784 |
| ensembl | rs29784 |
| geneview | rs29784 |
| scholar | rs29784 |
| rs29784 | |
| pharmgkb | rs29784 |
| gwascentral | rs29784 |
| openSNP | rs29784 |
| 23andMe | rs29784 |
| SNPshot | rs29784 |
| SNPdbe | rs29784 |
| MSV3d | rs29784 |
| GWAS Ctlg | rs29784 |
| GMAF | 0.3512 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22306654
] Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis
| GWAS snp | |
|---|---|
| PMID | [PMID 23989729]
|
| Trait | Infantile hypertrophic pyloric stenosis |
| Title | Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis. |
| Risk Allele | T |
| P-val | 8E-18 |
| Odds Ratio | 1.36 [1.27-1.46] |
