rs2704188
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2704188(C;C) |
| Make rs2704188(C;T) |
| Make rs2704188(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 58079484 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2704188 |
| dbSNP (classic) | rs2704188 |
| ClinGen | rs2704188 |
| ebi | rs2704188 |
| HLI | rs2704188 |
| Exac | rs2704188 |
| Gnomad | rs2704188 |
| Varsome | rs2704188 |
| LitVar | rs2704188 |
| Map | rs2704188 |
| PheGenI | rs2704188 |
| Biobank | rs2704188 |
| 1000 genomes | rs2704188 |
| hgdp | rs2704188 |
| ensembl | rs2704188 |
| geneview | rs2704188 |
| scholar | rs2704188 |
| rs2704188 | |
| pharmgkb | rs2704188 |
| gwascentral | rs2704188 |
| openSNP | rs2704188 |
| 23andMe | rs2704188 |
| SNPshot | rs2704188 |
| SNPdbe | rs2704188 |
| MSV3d | rs2704188 |
| GWAS Ctlg | rs2704188 |
| GMAF | 0.4096 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19886994
] ALDH1A2 (RALDH2) genetic variation in human congenital heart disease
