List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 42 by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001199799.2(ILDR1):c.686T>C (p.Leu229Pro)	rs546168333	0.00038
NM_001199799.2(ILDR1):c.866T>G (p.Leu289Trp)	rs141450561	0.00023
NM_001199799.2(ILDR1):c.1519G>A (p.Glu507Lys)
NM_001199799.2(ILDR1):c.758T>C (p.Met253Thr)

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