List of variants studied for autosomal recessive nonsyndromic hearing loss 4 by 3billion

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.919-2A>G	rs111033313	0.00018
NM_000441.2(SLC26A4):c.2168A>G (p.His723Arg)	rs121908362	0.00004
NM_000441.2(SLC26A4):c.1262A>C (p.Gln421Pro)	rs201660407	0.00003
NM_000441.2(SLC26A4):c.1149+3A>G	rs111033314	0.00002
NM_000441.2(SLC26A4):c.170C>A (p.Ser57Ter)	rs111033200	0.00001
NM_000441.2(SLC26A4):c.439A>G (p.Met147Val)	rs760413427	0.00001
NM_000441.2(SLC26A4):c.1337A>G (p.Gln446Arg)	rs768471577
NM_000441.2(SLC26A4):c.1586T>C (p.Ile529Thr)	rs786204739
NM_000441.2(SLC26A4):c.1803G>A (p.Lys601=)
NM_000441.2(SLC26A4):c.2028del (p.Arg677fs)	rs2129318300
NM_000441.2(SLC26A4):c.2145G>T (p.Lys715Asn)	rs397516427
NM_000441.2(SLC26A4):c.269C>T (p.Ser90Leu)	rs370588279
NM_000441.2(SLC26A4):c.412G>C (p.Val138Leu)	rs111033199
NM_000441.2(SLC26A4):c.416G>T (p.Gly139Val)	rs756272252
NM_000441.2(SLC26A4):c.617T>A (p.Leu206Ter)	rs2129311933
NM_000441.2(SLC26A4):c.716T>A (p.Val239Asp)	rs111033256

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