Variants in gene SUOX with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001032386.2(SUOX):c.1096C>T (p.Arg366Cys)	rs760901724	0.00002
NM_001032386.2(SUOX):c.1376G>A (p.Arg459Gln)	rs776356158	0.00002
NM_001032386.2(SUOX):c.1097G>A (p.Arg366His)	rs776690106	0.00001
NM_001032386.2(SUOX):c.650G>A (p.Arg217Gln)	rs121908007	0.00001
NM_001032386.2(SUOX):c.1388C>T (p.Ser463Phe)	rs1565799921
NM_001032386.2(SUOX):c.520del (p.Asp174fs)	rs1565798380

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