Variants in gene TJP2 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004817.4(TJP2):c.1000C>T (p.Arg334Ter)	rs1182781290
NM_004817.4(TJP2):c.2327del (p.Arg775_Leu776insTer)	rs1830379007
NM_004817.4(TJP2):c.239+1G>A	rs749237210
NM_004817.4(TJP2):c.2509C>T (p.Arg837Ter)	rs746830415

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