Variants with conflicting interpretations "likely pathogenic" from ISCA site 14 and "uncertain significance" from any submitter

Minimum review status of the submission from ISCA site 14:		Collection method of the submission from ISCA site 14:
Minimum review status of the other submission:		Collection method of the other submission:
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
GRCh38/hg38 15q11.2(chr15:22655582-23066575)x1
GRCh38/hg38 16p12.2(chr16:21826171-22396610)x1

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