List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 77 by Division of Human Genetics, Children's Hospital of Philadelphia

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001384474.1(LOXHD1):c.5802C>A (p.Asn1934Lys)	rs61733519	0.00316
NM_001384474.1(LOXHD1):c.1570C>T (p.Arg524Cys)	rs192376005	0.00295
NM_001384474.1(LOXHD1):c.2399T>A (p.Val800Glu)	rs755485250	0.00006
NM_001384474.1(LOXHD1):c.5740G>A (p.Gly1914Arg)	rs727504988	0.00006
NM_001384474.1(LOXHD1):c.3962G>C (p.Gly1321Ala)	rs573953982	0.00004
NM_001384474.1(LOXHD1):c.5115_5127dup (p.Glu1710fs)	rs1555669048

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