List of variants in gene SLC26A4 reported as uncertain significance by Molecular Diagnostics Lab, Nemours Children's Health, Delaware

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.441G>A (p.Met147Ile)	rs201905280	0.00037
NM_000441.2(SLC26A4):c.1678G>A (p.Asp560Asn)	rs759360026	0.00002
NM_000441.2(SLC26A4):c.1262A>G (p.Gln421Arg)	rs201660407
NM_000441.2(SLC26A4):c.633A>G (p.Ile211Met)

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