Variants with conflicting interpretations "drug response" from OMIM and "other" from any submitter

Minimum review status of the submission from OMIM:		Collection method of the submission from OMIM:
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
NM_000769.4(CYP2C19):c.681G>A (p.Pro227=)	rs4244285	0.16148
CYP2D6*4	rs3892097	0.14340
CYP2C9*3	rs1057910	0.04900
NM_000106.6(CYP2D6):c.775del (p.Arg259fs)	rs35742686	0.01277
CYP2D6*6	rs5030655	0.00883
NM_000769.1(CYP2C19):c.1A>G (p.Met1Val)	rs28399504	0.00156
NM_000769.1(CYP2C19):c.636G>A (p.Trp212Ter)	rs4986893	0.00149
NM_000769.1(CYP2C19):c.1297C>T (p.Arg433Trp)	rs56337013	0.00001
NM_000106.5(CYP2D6):c.505G>T (p.Gly169Ter)	rs5030865

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