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

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000601.6(HGF):c.482+1986_482+1988del	rs1788701297
NM_000601.6(HGF):c.482+1991_482+2000del
NM_000601.6(HGF):c.495G>A (p.Ser165=)	rs137853235

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