Variants with conflicting interpretations "drug response" from Medical Genetics Summaries and "other" from any submitter

Minimum review status of the submission from Medical Genetics Summaries:		Collection method of the submission from Medical Genetics Summaries:
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: 10

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HGVS	dbSNP	gnomAD frequency
CYP2D6*10	rs1065852	0.18675
CYP2D6*4	rs3892097	0.14340
CYP2C9*2	rs1799853	0.08975
CYP2D6*41	rs28371725	0.06736
CYP2C9*3	rs1057910	0.04900
CYP2D6*6	rs5030655	0.00883
CYP2C9*5	rs28371686	0.00342
CYP2C9*6	rs9332131
CYP2D6*17
UGT1A1*28	rs3064744

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