List of variants in gene HGF reported as benign for Autosomal recessive nonsyndromic hearing loss 39

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000601.6(HGF):c.1272-4A>G	rs1800793	0.76662
NM_000601.6(HGF):c.1891G>A (p.Val631Met)	rs145494248	0.00053
NM_000601.6(HGF):c.866-22del	rs5745686

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