Total variants with conflicting interpretations: 15
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_001348946. |
rs1128503 | 0.63165 |
NM_001348946. |
rs1045642 | 0.57896 |
NM_000106. |
rs1135840 | 0.42305 |
CYP2D6*10 | rs1065852 | 0.18675 |
CYP2D6*4 | rs3892097 | 0.14340 |
NM_001348946. |
rs9282564 | 0.07388 |
CYP2D6*41 | rs28371725 | 0.06736 |
NM_000106. |
rs769258 | 0.03995 |
NM_000106. |
rs28371717 | 0.00827 |
NM_000914. |
rs62638690 | 0.00573 |
NM_001074. |
rs61361928 | 0.00284 |
NM_000914. |
rs41292890 | 0.00226 |
NM_000106. |
rs5030656 | |
NM_000106. |
rs16947 | |
NM_001348946. |
rs2032582 |