List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 4; Pendred syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_012188.5(FOXI1):c.1088G>T (p.Ser363Ile)	rs150705492	0.00031
NM_012188.5(FOXI1):c.1090G>A (p.Val364Ile)	rs201090454	0.00022
NM_012188.5(FOXI1):c.1013C>T (p.Ala338Val)	rs367809742	0.00020
NM_000441.2(SLC26A4):c.1234G>A (p.Val412Ile)	rs111033527	0.00012
NM_000441.2(SLC26A4):c.2029C>T (p.Arg677Trp)	rs397516426	0.00010
NM_000441.2(SLC26A4):c.2291C>T (p.Thr764Met)	rs150597240	0.00010
NM_000441.2(SLC26A4):c.340G>A (p.Gly114Arg)	rs368844392	0.00008
NM_000441.2(SLC26A4):c.128G>A (p.Arg43His)	rs372116042	0.00006
NM_000441.2(SLC26A4):c.2234C>T (p.Thr745Met)	rs781300835	0.00005
NM_012188.5(FOXI1):c.773G>A (p.Gly258Glu)	rs121909340	0.00005
NM_000441.2(SLC26A4):c.2008G>A (p.Val670Ile)	rs201689637	0.00004
NM_000441.2(SLC26A4):c.1195T>C (p.Ser399Pro)	rs747431002	0.00003
NM_000441.2(SLC26A4):c.1301C>A (p.Ala434Asp)	rs1035397261	0.00003
NM_000441.2(SLC26A4):c.1409G>A (p.Arg470His)	rs200779286	0.00003
NM_012188.5(FOXI1):c.545A>G (p.Lys182Arg)	rs772882906	0.00003
NM_000441.2(SLC26A4):c.1678G>A (p.Asp560Asn)	rs759360026	0.00002
NM_000441.2(SLC26A4):c.2009T>C (p.Val670Ala)	rs200712253	0.00002
NM_000441.2(SLC26A4):c.803A>G (p.Asn268Ser)	rs200431470	0.00002
NM_012188.5(FOXI1):c.937G>C (p.Gly313Arg)	rs755810719	0.00002
NM_000441.2(SLC26A4):c.1124A>G (p.Tyr375Cys)	rs148425972	0.00001
NM_000441.2(SLC26A4):c.236G>A (p.Arg79Gln)	rs200706874	0.00001
NM_000441.2(SLC26A4):c.86A>G (p.Glu29Gly)	rs1446406563	0.00001
NM_012188.5(FOXI1):c.-18G>A	rs764490860	0.00001
NM_012188.5(FOXI1):c.763G>A (p.Ala255Thr)	rs951259617	0.00001
NM_000441.2(SLC26A4):c.1286C>A (p.Ala429Glu)	rs753269996
NM_000441.2(SLC26A4):c.2317G>A (p.Glu773Lys)	rs764791809
NM_012188.5(FOXI1):c.307G>T (p.Gly103Trp)	rs1053809070

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