Variants with conflicting interpretations "benign" from Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ and "drug response" from any submitter

Minimum review status of the submission from Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+:		Collection method of the submission from Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+:
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: 6

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HGVS	dbSNP	gnomAD frequency
NM_030667.3(PTPRO):c.1106-10T>A	rs4764199	0.84939
NM_000754.4(COMT):c.186C>T (p.His62=)	rs4633	0.44697
NM_000754.4(COMT):c.472G>A (p.Val158Met)	rs4680	0.44044
NM_000103.4(CYP19A1):c.*19C>T	rs10046	0.42803
NM_000754.4(COMT):c.408C>G (p.Leu136=)	rs4818	0.32165
NM_006446.5(SLCO1B1):c.521T>C (p.Val174Ala)	rs4149056	0.12106

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