rs7169289
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7169289(A;A) |
| Make rs7169289(A;G) |
| Make rs7169289(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 57951485 |
| Gene | ALDH1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7169289 |
| dbSNP (classic) | rs7169289 |
| ClinGen | rs7169289 |
| ebi | rs7169289 |
| HLI | rs7169289 |
| Exac | rs7169289 |
| Gnomad | rs7169289 |
| Varsome | rs7169289 |
| LitVar | rs7169289 |
| Map | rs7169289 |
| PheGenI | rs7169289 |
| Biobank | rs7169289 |
| 1000 genomes | rs7169289 |
| hgdp | rs7169289 |
| ensembl | rs7169289 |
| geneview | rs7169289 |
| scholar | rs7169289 |
| rs7169289 | |
| pharmgkb | rs7169289 |
| gwascentral | rs7169289 |
| openSNP | rs7169289 |
| 23andMe | rs7169289 |
| SNPshot | rs7169289 |
| SNPdbe | rs7169289 |
| MSV3d | rs7169289 |
| GWAS Ctlg | rs7169289 |
| GMAF | 0.2011 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20375987] A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid
[PMID 25293959
] Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects
