rs34005929
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs34005929(A;A) |
| Make rs34005929(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 61740835 |
| Gene | HIF1A, LOC105370526 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34005929 |
| dbSNP (classic) | rs34005929 |
| ClinGen | rs34005929 |
| ebi | rs34005929 |
| HLI | rs34005929 |
| Exac | rs34005929 |
| Gnomad | rs34005929 |
| Varsome | rs34005929 |
| LitVar | rs34005929 |
| Map | rs34005929 |
| PheGenI | rs34005929 |
| Biobank | rs34005929 |
| 1000 genomes | rs34005929 |
| hgdp | rs34005929 |
| ensembl | rs34005929 |
| geneview | rs34005929 |
| scholar | rs34005929 |
| rs34005929 | |
| pharmgkb | rs34005929 |
| gwascentral | rs34005929 |
| openSNP | rs34005929 |
| 23andMe | rs34005929 |
| SNPshot | rs34005929 |
| SNPdbe | rs34005929 |
| MSV3d | rs34005929 |
| GWAS Ctlg | rs34005929 |
| GMAF | 0.001837 |
| Max Magnitude | 0 |
[PMID 19691832
] Association of hypoxia inducible factor-1 alpha gene polymorphism with both type 1 and type 2 diabetes in a Caucasian (Hungarian) sample
[PMID 18980686] Non-synonymous sequence variants within the oxygen-dependent degradation domain of the HIF1A gene are not associated with pre-eclampsia in the Finnish population.
[PMID 19546348] Genetic variations in the hypoxia-inducible factor-1alpha gene and lung cancer.
