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

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

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.541G>T (p.Glu181Ter)	rs1198103383	0.00001
NM_006073.4(TRDN):c.502G>T (p.Glu168Ter)	rs545032318

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