List of variants in gene FH reported as likely pathogenic by Mayo Clinic Laboratories, Mayo Clinic

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000143.4(FH):c.1255T>C (p.Ser419Pro)	rs200004220	0.00001
NM_000143.4(FH):c.1067T>A (p.Leu356Ter)	rs727503927
NM_000143.4(FH):c.1097G>A (p.Ser366Asn)	rs863224004
NM_000143.4(FH):c.668_669del (p.Lys223fs)	rs886039364

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