rs573872
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs573872(G;G) |
| Make rs573872(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 153754374 |
| Gene | LOC105374165 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs573872 |
| dbSNP (classic) | rs573872 |
| ClinGen | rs573872 |
| ebi | rs573872 |
| HLI | rs573872 |
| Exac | rs573872 |
| Gnomad | rs573872 |
| Varsome | rs573872 |
| LitVar | rs573872 |
| Map | rs573872 |
| PheGenI | rs573872 |
| Biobank | rs573872 |
| 1000 genomes | rs573872 |
| hgdp | rs573872 |
| ensembl | rs573872 |
| geneview | rs573872 |
| scholar | rs573872 |
| rs573872 | |
| pharmgkb | rs573872 |
| gwascentral | rs573872 |
| openSNP | rs573872 |
| 23andMe | rs573872 |
| SNPshot | rs573872 |
| SNPdbe | rs573872 |
| MSV3d | rs573872 |
| GWAS Ctlg | rs573872 |
| GMAF | 0.2006 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | G |
| P-val | 5E-14 |
| Odds Ratio | 1.37 [1.26-1.48] |
