List of variants in gene FMO3 reported as pathogenic by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001002294.3(FMO3):c.769G>A (p.Val257Met)	rs1736557	0.06174
NM_001002294.3(FMO3):c.913G>T (p.Glu305Ter)	rs61753344	0.00035
NM_001002294.3(FMO3):c.1474C>T (p.Arg492Trp)	rs72549334	0.00019
NM_001002294.3(FMO3):c.1302G>A (p.Met434Ile)	rs72549332	0.00007
NM_001002294.3(FMO3):c.182A>G (p.Asn61Ser)	rs72549322	0.00003
NM_001002294.3(FMO3):c.198G>T (p.Met66Ile)	rs72549323	0.00001
NG_012690.2:g.4664_16889del
NM_001002294.3(FMO3):c.1160G>T (p.Arg387Leu)	rs72549331
NM_001002294.3(FMO3):c.154G>A (p.Ala52Thr)	rs72549321
NM_001002294.3(FMO3):c.192del (p.Glu65fs)
NM_001002294.3(FMO3):c.940G>T (p.Glu314Ter)	rs72549330
NM_001002294.3(FMO3):c.94G>A (p.Glu32Lys)	rs72549320

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