List of variants reported as benign for Pendred syndrome by ClinGen Hearing Loss Variant Curation Expert Panel

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.1708-18T>A	rs55701254	0.02432
NM_000441.2(SLC26A4):c.565G>T (p.Ala189Ser)	rs35045430	0.00378
NM_000441.2(SLC26A4):c.416-7T>C	rs111033387	0.00178
NM_000441.2(SLC26A4):c.1069G>A (p.Ala357Thr)	rs145467740	0.00166
NM_000441.2(SLC26A4):c.1363A>T (p.Ile455Phe)	rs375576481	0.00003

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