ClinVar Miner

Variants with conflicting interpretations "other" from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics and "drug response" from any submitter

Minimum review status of the submission from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics: Collection method of the submission from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 22
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HGVS dbSNP
CYP2C19*17 rs12248560
CYP2C19*3 rs4986893
CYP2C19*4A rs28399504
CYP2C19*5 rs56337013
CYP2C19*8 rs41291556
CYP2C9*2 rs1799853
CYP2C9*3 rs1057910
CYP2C9*5 rs28371686
CYP2C9*6 rs9332131
CYP2D6*10 rs1065852
CYP2D6*17 rs28371706
CYP2D6*4 rs3892097
CYP2D6*41 rs28371725
CYP2D6*6 rs5030655
NM_000041.2(APOE):c.526C>T (p.Arg176Cys) rs7412
NM_000106.5(CYP2D6):c.505G>T (p.Gly169Ter) rs5030865
NM_000106.5(CYP2D6):c.775delA (p.Arg259Glyfs) rs35742686
NM_000106.5(CYP2D6):c.841_843delAAG (p.Lys281del) rs5030656
NM_000769.1(CYP2C19):c.681G>A (p.Pro227=) rs4244285
NM_005957.5(MTHFR):c.665C>T (p.Ala222Val) rs1801133
NM_006446.5(SLCO1B1):c.521T>C (p.Val174Ala) rs4149056
Single allele

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