List of variants reported as likely pathogenic for SLC26A4-Related Disorders

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)	rs111033212	0.00077
NM_000441.2(SLC26A4):c.2171A>G (p.Asp724Gly)	rs757820624	0.00003
NM_000441.2(SLC26A4):c.554G>C (p.Arg185Thr)	rs542620119	0.00003
NM_000441.2(SLC26A4):c.1668T>A (p.Tyr556Ter)	rs1791846977

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