List of variants reported as uncertain significance for Hearing loss, autosomal dominant 82

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001001331.4(ATP2B2):c.2953G>A (p.Ala985Thr)	rs146069247	0.00005
NM_001001331.4(ATP2B2):c.1046A>G (p.Lys349Arg)	rs536636171	0.00003
NM_001001331.4(ATP2B2):c.1129A>C (p.Ser377Arg)
NM_001001331.4(ATP2B2):c.2336A>G (p.Asp779Gly)	rs2470208999
NM_001001331.4(ATP2B2):c.3059G>A (p.Arg1020His)
NM_001001331.4(ATP2B2):c.3487T>C (p.Ser1163Pro)
NM_001001331.4(ATP2B2):c.919G>A (p.Gly307Arg)	rs2061684217

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