Variants with conflicting interpretations "pathogenic" from Centogene AG - the Rare Disease Company and "pathogenic" from any submitter

Minimum review status of the submission from Centogene AG - the Rare Disease Company:		Collection method of the submission from Centogene AG - the Rare Disease Company:
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
NM_000784.4(CYP27A1):c.1184+1G>A	rs587778777	0.00009

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