Variants with conflicting interpretations "likely pathogenic" from Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine and "drug response" from any submitter

Minimum review status of the submission from Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine:		Collection method of the submission from Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine:
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: 1

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HGVS	dbSNP	gnomAD frequency
NC_012920.1:m.1494C>T	rs267606619

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