List of variants in gene HGF studied for Autosomal recessive nonsyndromic hearing loss 39

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000601.6(HGF):c.1272-4A>G	rs1800793	0.76662
NM_000601.6(HGF):c.1008G>A (p.Glu336=)	rs148714837	0.00202
NM_000601.6(HGF):c.1891G>A (p.Val631Met)	rs145494248	0.00053
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.482+1986_482+1988del	rs1788701297
NM_000601.6(HGF):c.482+1991_482+2000del
NM_000601.6(HGF):c.495G>A (p.Ser165=)	rs137853235
NM_000601.6(HGF):c.866-22del	rs5745686
NM_000601.6(HGF):c.983G>T (p.Arg328Leu)	rs374484762

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