List of variants reported as likely pathogenic for Trimethylaminuria

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001002294.3(FMO3):c.1474C>T (p.Arg492Trp)	rs72549334	0.00019
NM_001002294.3(FMO3):c.442G>A (p.Gly148Arg)	rs72549325	0.00010
NM_001002294.3(FMO3):c.929C>T (p.Ser310Leu)	rs572292275	0.00006
NM_001002294.3(FMO3):c.667C>T (p.Arg223Trp)	rs762600525	0.00004
NM_001002294.3(FMO3):c.182A>G (p.Asn61Ser)	rs72549322	0.00003
NM_001002294.3(FMO3):c.198G>T (p.Met66Ile)	rs72549323	0.00001
NM_001002294.3(FMO3):c.370C>T (p.Gln124Ter)	rs1384237868	0.00001
NM_001002294.3(FMO3):c.584C>T (p.Ser195Leu)
NM_001002294.3(FMO3):c.828-2A>G
NM_006894.4(FMO3):c.[472G>A;923A>G]

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