rs11228719
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11228719(C;C) |
| Make rs11228719(C;T) |
| Make rs11228719(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 56672760 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11228719 |
| dbSNP (classic) | rs11228719 |
| ClinGen | rs11228719 |
| ebi | rs11228719 |
| HLI | rs11228719 |
| Exac | rs11228719 |
| Gnomad | rs11228719 |
| Varsome | rs11228719 |
| LitVar | rs11228719 |
| Map | rs11228719 |
| PheGenI | rs11228719 |
| Biobank | rs11228719 |
| 1000 genomes | rs11228719 |
| hgdp | rs11228719 |
| ensembl | rs11228719 |
| geneview | rs11228719 |
| scholar | rs11228719 |
| rs11228719 | |
| pharmgkb | rs11228719 |
| gwascentral | rs11228719 |
| openSNP | rs11228719 |
| 23andMe | rs11228719 |
| SNPshot | rs11228719 |
| SNPdbe | rs11228719 |
| MSV3d | rs11228719 |
| GWAS Ctlg | rs11228719 |
| GMAF | 0.377 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22419666 ]
|
| Trait | |
| Title | Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. |
| Risk Allele | |
| P-val | 0.000004 |
| Odds Ratio | 1.6400 None |
