{{Rsnum
|rsid=1788776
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=18
|position=23664073
|Orientation=plus
|Gene=ANKRD29
|Gene_s=ANKRD29
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 29.2 | 50.8 | 20.0
| HCB | 17.8 | 46.7 | 35.6
| JPT | 22.7 | 43.2 | 34.1
| YRI | 49.2 | 42.9 | 7.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 17.8 | 46.7 | 35.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24256812
  |Trait=Amyotrophic lateral sclerosis (sporadic)
  |Title=A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
  |RiskAllele=A
  |Pval=8E-6
  |OR=1.11
  |ORtxt=[1.06-1.16]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}