ClinVar Miner

Variants with conflicting interpretations "other" and "drug response"

Submission 1 (other) minimum review status: Submission 1 (other) method:
Submission 2 (drug response) minimum review status: Submission 2 (drug response) method:
ClinVar version:

Total variants with conflicting interpretations: 24

HGVS dbSNP
NM_000041.2(APOE):c.526C>T (p.Arg176Cys) rs7412
NM_000106.5(CYP2D6):c.454delT (p.Trp152Glyfs) rs5030655
NM_000106.5(CYP2D6):c.505G>T (p.Gly169Ter) rs5030865
NM_000106.5(CYP2D6):c.506-1G>A rs3892097
NM_000106.5(CYP2D6):c.775delA (p.Arg259Glyfs) rs35742686
NM_000106.6(CYP2D6):c.100C>T (p.Pro34Ser) rs1065852
NM_000110.3(DPYD):c.2846A>T (p.Asp949Val) rs67376798
NM_000367.4(TPMT):c.460G>A (p.Ala154Thr) rs1800460
NM_000367.4(TPMT):c.719A>G (p.Tyr240Cys) rs1142345
NM_000402.4(G6PD):c.292G>A (p.Val98Met) rs1050828
NM_000769.1(CYP2C19):c.-806C>T rs12248560
NM_000769.1(CYP2C19):c.1297C>T (p.Arg433Trp) rs56337013
NM_000769.1(CYP2C19):c.1A>G (p.Met1Val) rs28399504
NM_000769.1(CYP2C19):c.358T>C (p.Trp120Arg) rs41291556
NM_000769.1(CYP2C19):c.636G>A (p.Trp212Ter) rs4986893
NM_000769.1(CYP2C19):c.681G>A (p.Pro227=) rs4244285
NM_000771.3(CYP2C9):c.1075A>C (p.Ile359Leu) rs1057910
NM_000771.3(CYP2C9):c.430C>T (p.Arg144Cys) rs1799853
NM_000771.4(CYP2C9):c.1080C>G (p.Asp360Glu) rs28371686
NM_005957.4(MTHFR):c.665C>T (p.Ala222Val) rs1801133
NM_006446.4(SLCO1B1):c.521T>C (p.Val174Ala) rs4149056
NM_024006.4(VKORC1):c.-1639G>A rs9923231
UGT1A1*28 rs3064744
UGT1A1*6 rs4148323

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