Variants in gene SLC26A2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_000112.4(SLC26A2):c.*4799G>A	rs72832119	0.01211
NM_000112.4(SLC26A2):c.*4930C>T	rs79521091	0.00981
NM_000112.4(SLC26A2):c.987T>C (p.Leu329=)	rs116302615	0.00246
NM_000112.4(SLC26A2):c.2087A>G (p.Asn696Ser)	rs34351171	0.00214
NM_000112.4(SLC26A2):c.1046T>A (p.Phe349Tyr)	rs114212275	0.00073
NM_000112.4(SLC26A2):c.229A>C (p.Asn77His)	rs76784312	0.00025
NM_000112.4(SLC26A2):c.1512G>A (p.Met504Ile)	rs76668544	0.00022
NM_000112.4(SLC26A2):c.1761C>T (p.Leu587=)	rs745590895	0.00009
NM_000112.4(SLC26A2):c.1194A>T (p.Val398=)	rs886038240	0.00005

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