List of variants reported as uncertain significance for Autosomal dominant nonsyndromic hearing loss 11 by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.1007G>A (p.Arg336His)	rs45629132	0.00164
NM_000260.4(MYO7A):c.1132C>T (p.Arg378Cys)	rs199818783	0.00024
NM_000260.4(MYO7A):c.3750+20C>T	rs577104822	0.00005
NM_000260.4(MYO7A):c.3375+3G>A	rs397516299	0.00001
NM_000260.4(MYO7A):c.359G>A (p.Arg120His)	rs369493667	0.00001
NM_000260.4(MYO7A):c.6362C>T (p.Thr2121Met)	rs769205075	0.00001
NM_000260.4(MYO7A):c.1817G>A (p.Arg606His)	rs782311929
NM_000260.4(MYO7A):c.2617C>T (p.Arg873Trp)	rs200454015
NM_000260.4(MYO7A):c.5982G>A (p.Met1994Ile)	rs1957644487

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