List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 42

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001199799.2(ILDR1):c.1297C>T (p.Arg433Trp)	rs140567004	0.00050
NM_001199799.2(ILDR1):c.686T>C (p.Leu229Pro)	rs546168333	0.00038
NM_001199799.2(ILDR1):c.1184T>C (p.Leu395Ser)	rs143311654	0.00037
NM_001199799.2(ILDR1):c.866T>G (p.Leu289Trp)	rs141450561	0.00023
NM_001199799.2(ILDR1):c.1312C>T (p.Pro438Ser)	rs554966703	0.00008
NM_001199799.2(ILDR1):c.1291C>T (p.Arg431Cys)	rs376510686	0.00001
NM_001199799.2(ILDR1):c.1291_1305delinsGTGAGG (p.Arg431_Ser435delinsValArg)
NM_001199799.2(ILDR1):c.1301C>T (p.Pro434Leu)	rs760257421
NM_001199799.2(ILDR1):c.1358G>A (p.Arg453Gln)
NM_001199799.2(ILDR1):c.1519G>A (p.Glu507Lys)
NM_001199799.2(ILDR1):c.758T>C (p.Met253Thr)
NM_001199799.2(ILDR1):c.779-6A>G

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