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  • SCN5A
    • Premature Ventricular Contraction
    • Cardiomyopathy, Dilated, 1e
    • Enamel-Renal Syndrome
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
    • Ventricular Fibrillation, Paroxysmal Familial, 1
  • TTN
    • Premature Ventricular Contraction
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • RYR2
    • Premature Ventricular Contraction
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
    • Ventricular Fibrillation, Paroxysmal Familial, 1
  • TTPA
    • Familial Isolated Vitamin E Deficiency
  • LMNA
    • Premature Ventricular Contraction
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • DES
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • SLC12A6
    • Andermann Syndrome
  • TRDN
    • Premature Ventricular Contraction
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
  • PQBP1
    • Renpenning's Syndrome
  • MED12
    • Fg Syndrome
  • FAM20A
    • Enamel-Renal Syndrome
  • SLC17A5
    • Salla Disease
  • NGLY1
    • Ngly1 Deficiency
  • UBE3B
    • Kaufman Oculocerebrofacial Syndrome
  • CALM1
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
    • Ventricular Fibrillation, Paroxysmal Familial, 1
  • SGCD
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • CASQ2
    • Premature Ventricular Contraction
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
  • IFIH1
    • Singleton Merten Syndrome
  • TCAP
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • FKTN
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy

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