{{Rsnum
|rsid=516514
|Gene=FHOD3
|Chromosome=18
|position=36681085
|Orientation=plus
|GMAF=0.4848
|Gene_s=FHOD3
|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 | 23.2 | 54.5 | 22.3
| HCB | 15.4 | 47.1 | 37.5
| JPT | 19.5 | 46.0 | 34.5
| YRI | 23.8 | 52.4 | 23.8
| ASW | 29.8 | 35.1 | 35.1
| CHB | 15.4 | 47.1 | 37.5
| CHD | 10.2 | 39.8 | 50.0
| GIH | 36.6 | 45.5 | 17.8
| LWK | 23.6 | 57.3 | 19.1
| MEX | 19.6 | 57.1 | 23.2
| MKK | 14.2 | 54.2 | 31.6
| TSI | 29.7 | 43.6 | 26.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=23255317
|Title=Formin Homology 2 Domain Containing 3 (FHOD3) Variants Associated with Hypertrophic Cardiomyopathy
|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 | FTDNA}}
{{on chip | Illumina Human 1M}}