{{Rsnum
|rsid=61753344
|Gene=FMO3
|Chromosome=1
|position=171114092
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=FMO3
}}{{omim
|id=136132
|rsnum=61753344
|variant=0001
}}

[[rs61753344]] is a SNP in the [[FMO3]] gene. It has been reported in both homozygous and heterozygous forms to potentially be linked to [[trimethylaminuria]]; in the homozygous form, it has also been linked to [[tachycardia]] and severe [[hypertension]] after eating cheese (which contains tyramine) and after using nasal [[epinephrine]].{{PMID|987532}}
{{ClinVar
|rsid=61753344
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=171114092
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050368000605040016110100
|GENEINFO=FMO3:2328
|GENE_NAME=FMO3
|GENE_ID=2328
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.171114092G>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001002294.2:c.913G>T; NBK1103; 136132.0001
|CLNSIG=5
|CLNCUI=C0342739; C0342739
|CLNDBN=Trimethylaminuria
|Disease=Trimethylaminuria
|CLNACC=RCV000017697.26
|Tags=PM;PMC;S3D;SLO;NSN;REF;ASP;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1103:C0342739:602079:237959005
|COMMON=0
}}

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}