List of variants in gene SLC26A4 reported as likely benign for Autosomal recessive nonsyndromic hearing loss 4; Pendred syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.1826T>G (p.Val609Gly)	rs17154335	0.04399
NM_000441.2(SLC26A4):c.970A>T (p.Asn324Tyr)	rs36039758	0.01056
NM_000441.2(SLC26A4):c.1790T>C (p.Leu597Ser)	rs55638457	0.00545
NM_000441.2(SLC26A4):c.898A>C (p.Ile300Leu)	rs111033304	0.00450
NM_000441.2(SLC26A4):c.990C>T (p.Ser330=)	rs770874403	0.00004
NM_000441.2(SLC26A4):c.1363A>T (p.Ile455Phe)	rs375576481	0.00003
NM_000441.2(SLC26A4):c.768G>A (p.Thr256=)	rs552050976	0.00001

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