List of variants in gene combination LOC123956210, SLC26A4 reported as benign for 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.2130C>T (p.Asp710=)	rs17154347	0.02079
NM_000441.2(SLC26A4):c.2139T>G (p.Ile713Met)	rs143708308	0.00268
NM_000441.2(SLC26A4):c.2190G>T (p.Gln730His)	rs142723249	0.00092
NM_000441.2(SLC26A4):c.2090-59AAAC[3]	rs112211967

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