List of variants in gene SLC26A4 reported as pathogenic by Laboratory of Human Genetics, Institute of Biosciences - University of Sao Paulo

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.1246A>C (p.Thr416Pro)	rs28939086	0.00019
NM_000441.2(SLC26A4):c.84C>A (p.Ser28Arg)	rs539699299	0.00001
NM_000441.2(SLC26A4):c.1554G>A (p.Trp518Ter)	rs727503428

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