{{Rsnum
|rsid=28363581
|Gene=FMO3
|Chromosome=1
|position=171114258
|Orientation=plus
|GMAF=0.001377
|Gene_s=FMO3
|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 | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{ClinVar
|rsid=28363581
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=171114258
|CHROM=1
|GMAF=0.0014
|dbSNPBuildID=125
|SSR=0
|SAO=1
|VP=0x050370000a05040517110100
|GENEINFO=FMO3:2328
|GENE_NAME=FMO3
|GENE_ID=2328
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.171114258T>C
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=602079
|CLNDBN=Trimethylaminuria
|Tags=PM;TPA;S3D;SLO;NSM;REF;ASP;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9986; 0.001377
|CLNACC=RCV000020652.1
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1103:C0342739:602079:237959005
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_001002294.2:c.1079T>C; NBK1103
|COMMON=1
|Disease=Trimethylaminuria
}}

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