List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 4 by Precision Medicine Center, Zhengzhou University

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.439A>G (p.Met147Val)	rs760413427	0.00001
NM_000441.2(SLC26A4):c.1264-12T>A	rs2129316889
NM_000441.2(SLC26A4):c.1299dup (p.Ala434fs)	rs2129316898
NM_000441.2(SLC26A4):c.1786C>T (p.Gln596Ter)	rs1476190682
NM_000441.2(SLC26A4):c.1991C>T (p.Ala664Val)	rs2129318281
NM_000441.2(SLC26A4):c.2000T>C (p.Phe667Ser)	rs121908360
NM_000441.2(SLC26A4):c.2167C>G (p.His723Asp)	rs1417146153
NM_000441.2(SLC26A4):c.317C>A (p.Ala106Asp)	rs1562822565
NM_000441.2(SLC26A4):c.387del (p.Phe130fs)	rs2129311265
NM_000441.2(SLC26A4):c.415+2T>C	rs2129311282
NM_000441.2(SLC26A4):c.754T>C (p.Ser252Pro)	rs1315422549

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