{{Rsnum
|rsid=2303510
|Gene=FHOD3
|Chromosome=18
|position=36744128
|Orientation=minus
|GMAF=0.3333
|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 | 50.9 | 41.1 | 8.0
| HCB | 41.2 | 47.8 | 11.0
| JPT | 38.1 | 48.7 | 13.3
| YRI | 38.6 | 46.9 | 14.5
| ASW | 40.4 | 42.1 | 17.5
| CHB | 41.2 | 47.8 | 11.0
| CHD | 51.4 | 43.1 | 5.5
| GIH | 27.7 | 43.6 | 28.7
| LWK | 34.5 | 50.0 | 15.5
| MEX | 36.8 | 49.1 | 14.0
| MKK | 35.9 | 48.1 | 16.0
| TSI | 49.0 | 39.2 | 11.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=23255317
|Title=Formin Homology 2 Domain Containing 3 (FHOD3) Variants Associated with Hypertrophic Cardiomyopathy
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}