C1708350[trait identifier] AND "Mendelics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 42095	NM_000143.4(FH):c.1431_1433dup (p.Lys477dup)	FH	Duplication (inframe_insertion)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 296866	NM_000143.4(FH):c.1237-50TC[21]	FH	Microsatellite (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 296865	NM_000143.4(FH):c.1237-50TC[20]	FH	Microsatellite (intron variant)	Fumarase deficiency +4 more	GConflicting classifications of pathogenicity

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