{{Rsnum
|rsid=2163870
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=8
|Orientation=plus
|Gene=ANGPT1
|position=107365673
|Gene_s=ANGPT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 39.8 | 46.9 | 13.3
| HCB | 29.2 | 46.7 | 24.1
| JPT | 22.1 | 44.2 | 33.6
| YRI | 72.1 | 25.9 | 2.0
| ASW | 66.7 | 29.8 | 3.5
| CHB | 29.2 | 46.7 | 24.1
| CHD | 30.3 | 52.3 | 17.4
| GIH | 36.6 | 47.5 | 15.8
| LWK | 61.8 | 30.9 | 7.3
| MEX | 44.8 | 53.4 | 1.7
| MKK | 69.7 | 27.7 | 2.6
| TSI | 40.6 | 47.5 | 11.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24315451
  |Trait=Fractional exhaled nitric oxide (childhood)
  |Title=Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants.
  |RiskAllele=G
  |Pval=3E-6
  |OR=.06
  |ORtxt=[0.033-0.081] unit increase
  }}

{{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}}