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

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000601.6(HGF):c.724C>T (p.Arg242Trp)	rs202185530	0.00006
NM_000601.6(HGF):c.6G>T (p.Trp2Cys)	rs745851853	0.00001
NM_000601.6(HGF):c.1810T>C (p.Cys604Arg)
NM_000601.6(HGF):c.983G>T (p.Arg328Leu)	rs374484762

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