Related gene-specific medical variations for Gene (Select 3082) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 995374	NM_000601.6(HGF):c.1295C>T (p.Ala432Val)	HGF (A427V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 685592	GRCh37/hg19 7q21.11(chr7:81075835-81387108)x3	HGF	Copy number gain	not provided	GUncertain significance
Select item 256717	NM_000601.6(HGF):c.483-20G>A	HGF	Single nucleotide variant (intron variant)	not specified	GLikely benign

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