Variants with conflicting interpretations "uncertain significance" from Neuberg Centre For Genomic Medicine, NCGM and "likely pathogenic" from Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University

Minimum review status of the submission from Neuberg Centre For Genomic Medicine, NCGM:		Collection method of the submission from Neuberg Centre For Genomic Medicine, NCGM:
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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_000104.4(CYP1B1):c.1103G>A (p.Arg368His)	rs79204362	0.00125

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