{{Rsnum
|rsid=17589516
|Gene=ZFAND3
|Chromosome=6
|position=38068644
|Orientation=plus
|GMAF=0.03581
|Gene_s=ZFAND3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 89.4 | 10.6 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 96.5 | 3.5 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 80.2 | 18.8 | 1.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 87.9 | 12.1 | 0.0
| MKK | 94.2 | 5.8 | 0.0
| TSI | 79.4 | 20.6 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21901158
|Trait=None
|Title=Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
|RiskAllele=C
|Pval=0.000004
|OR=45.0000
|ORtxt=[24.00 - 69.00] % increase
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}