List of variants in gene SLC26A2 reported as uncertain significance by Genome Diagnostics Laboratory, The Hospital for Sick Children

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_000112.4(SLC26A2):c.1081G>A (p.Ala361Thr)	rs139051143	0.00026
NM_000112.4(SLC26A2):c.1487G>A (p.Arg496His)	rs150314895	0.00009
NM_000112.4(SLC26A2):c.1085G>T (p.Gly362Val)	rs1215069127	0.00001
NM_000112.4(SLC26A2):c.1442G>C (p.Ser481Thr)	rs1755089465
NM_000112.4(SLC26A2):c.1443T>C (p.Ser481=)	rs1054014161
NM_000112.4(SLC26A2):c.395T>C (p.Leu132Pro)	rs1755026324

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