{{Rsnum
|rsid=2274788
|Gene=ARHGAP29
|Chromosome=1
|position=94209170
|Orientation=plus
|GMAF=0.208
|Gene_s=ARHGAP29
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 36.3 | 55.8
| HCB | 10.2 | 46.7 | 43.1
| JPT | 6.3 | 34.2 | 59.5
| YRI | 0.0 | 4.1 | 95.9
| ASW | 0.0 | 15.8 | 84.2
| CHB | 10.2 | 46.7 | 43.1
| CHD | 11.0 | 52.3 | 36.7
| GIH | 5.0 | 15.0 | 80.0
| LWK | 0.0 | 6.4 | 93.6
| MEX | 1.7 | 37.9 | 60.3
| MKK | 2.6 | 26.3 | 71.2
| TSI | 4.9 | 37.3 | 57.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23400010
  |Trait=Thiazide-induced adverse metabolic effects in hypertensive patients
  |Title=Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans.
  |RiskAllele=C
  |Pval=1E-6
  |OR=23.07
  |ORtxt=[13.8-32.34] mg/dL decrease
  |OA=1
}}

{{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}}