rs3809922
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3809922(C;C) |
| Make rs3809922(C;T) |
| Make rs3809922(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 48921759 |
| Gene | SMAD7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3809922 |
| dbSNP (classic) | rs3809922 |
| ClinGen | rs3809922 |
| ebi | rs3809922 |
| HLI | rs3809922 |
| Exac | rs3809922 |
| Gnomad | rs3809922 |
| Varsome | rs3809922 |
| LitVar | rs3809922 |
| Map | rs3809922 |
| PheGenI | rs3809922 |
| Biobank | rs3809922 |
| 1000 genomes | rs3809922 |
| hgdp | rs3809922 |
| ensembl | rs3809922 |
| geneview | rs3809922 |
| scholar | rs3809922 |
| rs3809922 | |
| pharmgkb | rs3809922 |
| gwascentral | rs3809922 |
| openSNP | rs3809922 |
| 23andMe | rs3809922 |
| SNPshot | rs3809922 |
| SNPdbe | rs3809922 |
| MSV3d | rs3809922 |
| GWAS Ctlg | rs3809922 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24039762
] Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population
