List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 8 by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001256317.3(TMPRSS3):c.1042G>A (p.Asp348Asn)	rs111033261	0.00071
NM_001256317.3(TMPRSS3):c.280G>A (p.Gly94Arg)	rs143762350	0.00011
NM_001256317.3(TMPRSS3):c.1169C>T (p.Thr390Met)	rs145766262	0.00006
NM_001256317.3(TMPRSS3):c.764C>T (p.Ala255Val)	rs758738833	0.00002
NM_001256317.3(TMPRSS3):c.496C>T (p.Arg166Trp)	rs781395690	0.00001

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