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  • SCN5A
    • Premature Ventricular Contraction
    • Cardiomyopathy, Dilated, 1e
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
    • Ventricular Fibrillation, Paroxysmal Familial, 1
  • TTN
    • Premature Ventricular Contraction
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • CACNA1F
    • Oguchi Disease 1
    • X-Linked Congenital Stationary Night Blindness
    • Achromatopsia
  • CNGA3
    • Color Blindness
    • X-Linked Congenital Stationary Night Blindness
    • Achromatopsia
    • Oligocone Trichromacy
  • PAX3
    • Waardenburg Syndrome Type I
    • Heterochromia Iridum
  • CNGB3
    • Color Blindness
    • Achromatopsia
  • GNAT2
    • Color Blindness
    • Achromatopsia
  • ATF6
    • Color Blindness
    • Achromatopsia
  • RYR2
    • Premature Ventricular Contraction
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
    • Ventricular Fibrillation, Paroxysmal Familial, 1
  • PDE6H
    • Color Blindness
    • Achromatopsia
  • LMNA
    • Premature Ventricular Contraction
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • CYP4V2
    • Bietti Crystalline Dystrophy
  • LAMP2
    • Danon Disease
  • SAG
    • Oguchi Disease 1
    • X-Linked Congenital Stationary Night Blindness
  • DES
    • Cardiomyopathy, Dilated, 1e
    • Limb–girdle Muscular Dystrophy
  • NAA10
    • Premature Ventricular Contraction
    • Ogden Syndrome
  • SLC45A2
    • Oculocutaneous Albinism Type 4
    • Ocular Albinism, X-Linked
  • PDE6C
    • Achromatopsia
  • TRDN
    • Premature Ventricular Contraction
    • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
  • GPR143
    • Ocular Albinism, X-Linked

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