List of variants reported as uncertain significance for Hearing loss, autosomal dominant 73

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001145026.2(PTPRQ):c.6299T>G (p.Met2100Arg)	rs1330487603	0.00001
NM_001145026.2(PTPRQ):c.1331A>G (p.Glu444Gly)
NM_001145026.2(PTPRQ):c.1990+1G>C
NM_001145026.2(PTPRQ):c.386T>G (p.Ile129Ser)	rs1555180294
NM_001145026.2(PTPRQ):c.3974A>T (p.Asn1325Ile)
NM_001145026.2(PTPRQ):c.5606A>G (p.Gln1869Arg)	rs1275679740
NM_001145026.2(PTPRQ):c.5893C>A (p.Leu1965Met)
NM_001145026.2(PTPRQ):c.6881G>A (p.Trp2294Ter)	rs1555214288

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