{{Rsnum
|rsid=72549326
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FMO3
|position=171107811
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FMO3
}}[[rs72549326]], also known as Pro153Leu, is a SNP in the [[FMO3]] gene. Homozygous minor genotypes for this SNP have been reported to have [[trimethylaminuria]].{{PMID|8654418}}
{{omim
|id=136132
|rsnum=72549326
|variant=0004
}}{{ClinVar
|rsid=72549326
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=171107811
|CHROM=1
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050368000a05040002110100
|GENEINFO=FMO3:2328
|GENE_NAME=FMO3
|GENE_ID=2328
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.171107811C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001002294.2:c.458C>T; NBK1103; 136132.0004
|CLNSIG=5
|CLNCUI=C0342739; C0342739
|CLNDBN=Trimethylaminuria
|Disease=Trimethylaminuria
|CLNACC=RCV000017701.26
|Tags=PM;PMC;S3D;SLO;NSM;REF;ASP;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1103:C0342739:602079:237959005
}}{{PMID Auto
|PMID=9398858
|Title=Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome.
}}

{{PMID Auto
|PMID=9536088
|Title=Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.
}}

{{PMID Auto
|PMID=11191884
|Title=Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndrome.
}}