{{Rsnum
|rsid=12434438
|Gene=HIF1A
|Chromosome=14
|position=61730580
|Orientation=plus
|GMAF=0.3701
|Gene_s=HIF1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 71.7 | 25.7 | 2.7
| HCB | 59.1 | 35.8 | 5.1
| JPT | 56.6 | 38.9 | 4.4
| YRI | 2.1 | 15.8 | 82.2
| ASW | 7.0 | 38.6 | 54.4
| CHB | 59.1 | 35.8 | 5.1
| CHD | 54.1 | 38.5 | 7.3
| GIH | 44.6 | 41.6 | 13.9
| LWK | 1.8 | 32.7 | 65.5
| MEX | 62.1 | 31.0 | 6.9
| MKK | 10.9 | 37.8 | 51.3
| TSI | 36.3 | 47.1 | 16.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=24232601
|Title=Lack of association between the polymorphisms of hypoxia-inducible factor 1A (HIF1A) gene and SLE susceptibility in a Chinese population
}}

{{PMID Auto
|PMID=19306159
|Title=Association of hypoxia-inducible factor 1A (HIF1A) gene polymorphisms with systemic sclerosis in a French European Caucasian population.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}