List of variants in gene SLC26A4 reported as pathogenic by Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.626G>T (p.Gly209Val)	rs111033303	0.00037
NM_000441.2(SLC26A4):c.-3-2A>G	rs397516411	0.00025
NM_000441.2(SLC26A4):c.412G>T (p.Val138Phe)	rs111033199	0.00018
NM_000441.2(SLC26A4):c.2015G>A (p.Gly672Glu)	rs111033309	0.00010
NM_000441.2(SLC26A4):c.2T>C (p.Met1Thr)	rs111033302	0.00008
NM_000441.2(SLC26A4):c.716T>A (p.Val239Asp)	rs111033256	0.00005

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