{{Rsnum
|rsid=3776331
|Gene=ARHGAP26
|Chromosome=5
|position=143062229
|Orientation=minus
|GMAF=0.2681
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ARHGAP26
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 46.9 | 46.0
| HCB | 9.6 | 40.4 | 50.0
| JPT | 14.3 | 47.3 | 38.4
| YRI | 2.8 | 31.7 | 65.5
| ASW | 1.8 | 28.1 | 70.2
| CHB | 9.6 | 40.4 | 50.0
| CHD | 8.3 | 37.6 | 54.1
| GIH | 29.0 | 48.0 | 23.0
| LWK | 1.8 | 19.3 | 78.9
| MEX | 19.0 | 51.7 | 29.3
| MKK | 4.5 | 40.0 | 55.5
| TSI | 9.9 | 32.7 | 57.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18759275
|Trait=Serum uric acid
|Title=Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish
|RiskAllele=
|Pval=0.0000079999999999999996
|OR=0.30
|ORtxt=[NR] mg/dl increase in uric acid levels
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3776331
|overall_frequency_n=95
|overall_frequency_d=128
|overall_frequency=0.742188
|n_genomes=53
|n_genomes_annotated=0
|n_haplomes=83
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}