Variants in gene CYP2D6 with conflicting interpretations "other" and "likely benign"

Submission 1 (other) minimum review status:		Submission 1 (other) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
CYP2D6*10	rs1065852	0.18675
CYP2D6*4	rs3892097	0.14340
CYP2D6*41	rs28371725	0.06736
NM_000106.6(CYP2D6):c.1012G>A (p.Val338Met)	rs59421388	0.02682
NM_000106.6(CYP2D6):c.775del (p.Arg259fs)	rs35742686	0.01277
CYP2D6*6	rs5030655	0.00883
NM_000106.5(CYP2D6):c.971A>C (p.His324Pro)	rs5030867	0.00027
NM_000106.5(CYP2D6):c.124G>A (p.Gly42Arg)	rs5030862	0.00024
CYP2D6*17	rs28371706
NM_000106.5(CYP2D6):c.*264G>A (p.Gly169Arg)	rs5030865
NM_000106.5(CYP2D6):c.505G>T (p.Gly169Ter)	rs5030865
NM_000106.6(CYP2D6):c.841_843del (p.Lys281del)	rs5030656
Single allele

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