Variants with conflicting interpretations "pathogenic" from Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard and "benign" from any submitter

Minimum review status of the submission from Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard:		Collection method of the submission from Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard:
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
Single allele

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