List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 18B by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001292063.2(OTOG):c.7693+1G>A	rs548496846	0.00091
NM_001292063.2(OTOG):c.5966C>G (p.Ala1989Gly)	rs577901245	0.00038
NM_001292063.2(OTOG):c.7380T>A (p.Asp2460Glu)	rs532385451	0.00026
NM_001292063.2(OTOG):c.292+4A>C	rs535970426	0.00021
NM_001292063.2(OTOG):c.1184A>C (p.Gln395Pro)	rs876657936	0.00019
NM_001292063.2(OTOG):c.6181G>A (p.Val2061Met)	rs748497956	0.00018
NM_001292063.2(OTOG):c.8345C>T (p.Thr2782Met)	rs188322721	0.00013
NM_001292063.2(OTOG):c.8119G>A (p.Val2707Met)	rs566656846	0.00005
NM_001292063.2(OTOG):c.2080G>A (p.Ala694Thr)	rs757854202	0.00004
NM_001292063.2(OTOG):c.2084C>T (p.Ser695Phe)	rs1430140899
NM_001292063.2(OTOG):c.6179G>A (p.Arg2060His)	rs188527711

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