{{Rsnum
|rsid=11712165
|Gene=ARHGAP31
|Chromosome=3
|position=119399949
|Orientation=plus
|GMAF=0.3035
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=ARHGAP31
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 15.0 | 52.2 | 32.7
| HCB | 13.2 | 54.4 | 32.4
| JPT | 24.8 | 46.0 | 29.2
| YRI | 0.0 | 0.0 | 100.0
| ASW | 3.5 | 15.8 | 80.7
| CHB | 13.2 | 54.4 | 32.4
| CHD | 17.4 | 50.5 | 32.1
| GIH | 12.9 | 41.6 | 45.5
| LWK | 0.0 | 2.7 | 97.3
| MEX | 15.5 | 51.7 | 32.8
| MKK | 0.0 | 10.9 | 89.1
| TSI | 12.7 | 47.1 | 40.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20190752
|Trait=Celiac disease
|Title=Multiple common variants for celiac disease influencing immune gene expression
|RiskAllele=C
|Pval=8E-9
|OR=1.13
|ORtxt=[1.08-1.17]
|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 | Illumina Human 1M}}