rs11712066
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11712066(A;A) |
| Make rs11712066(A;G) |
| Make rs11712066(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 152112520 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11712066 |
| dbSNP (classic) | rs11712066 |
| ClinGen | rs11712066 |
| ebi | rs11712066 |
| HLI | rs11712066 |
| Exac | rs11712066 |
| Gnomad | rs11712066 |
| Varsome | rs11712066 |
| LitVar | rs11712066 |
| Map | rs11712066 |
| PheGenI | rs11712066 |
| Biobank | rs11712066 |
| 1000 genomes | rs11712066 |
| hgdp | rs11712066 |
| ensembl | rs11712066 |
| geneview | rs11712066 |
| scholar | rs11712066 |
| rs11712066 | |
| pharmgkb | rs11712066 |
| gwascentral | rs11712066 |
| openSNP | rs11712066 |
| 23andMe | rs11712066 |
| SNPshot | rs11712066 |
| SNPdbe | rs11712066 |
| MSV3d | rs11712066 |
| GWAS Ctlg | rs11712066 |
| GMAF | 0.1019 |
| 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 | A |
| P-val | 3E-21 |
| Odds Ratio | 1.55 [1.42-1.70] |
