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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000112.4(SLC26A2):c.2065A>T (p.Thr689Ser)	rs3776070	0.19906
NM_000112.4(SLC26A2):c.*1892dup	rs148778566	0.04587
NM_000112.4(SLC26A2):c.1474C>T (p.Arg492Trp)	rs78676079	0.01642
NM_000112.4(SLC26A2):c.2220A>G (p.Ter740=)	rs61732052	0.01353
NM_000112.4(SLC26A2):c.655A>G (p.Ile219Val)	rs35919114	0.00795
NM_000112.4(SLC26A2):c.*83T>G	rs143847430	0.00356
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.*600G>T	rs143723255	0.00148
NM_000112.4(SLC26A2):c.229A>C (p.Asn77His)	rs76784312	0.00025
NM_000112.4(SLC26A2):c.1410A>G (p.Val470=)	rs115777661	0.00017

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