"Clinical Genetics, Academic Medical Center"[submitter] AND "HGF"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 43607	NM_000601.6(HGF):c.1272-4A>G	HGF	Single nucleotide variant (intron variant)	Nonsyndromic Hearing Loss, Mixed +3 more	GBenign/Likely benign
Select item 43606	NM_000601.6(HGF):c.1008G>A (p.Glu336=)	HGF	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 779919	NM_000601.6(HGF):c.885C>T (p.Asp295=)	HGF	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign

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