• Eyes: Brown
• Hair: Dark Brown
• Height: 6'04"
• Weight (lbs): 200
• Blood: O Rh+
• CMV: +
• Ethnicity: Caucasian, Norwegian, Scottish
• Jewish Ancestry: No
• Education/Occupation: B.S. Computer Science / Student
• Live Birth / Pregnancy Confirmed: Yes

Test Results

• Extended Testing: Counsyl Fundamental Panel Plus (at least 21 conditions)
• Carrier For:
  • No disease causing mutations detected
• Results for Karyotyping / Spinal Muscular Atrophy:
  • Spinal Muscular Atrophy: Copy number 2
• Results with No Disease Causing Mutations: View full list
  • Karyotyping
  • Cystic Fibrosis
  • ABCC8-related Hyperinsulinism
  • Alpha-1 Antitrypsin Deficiency
  • Alpha Thalassemia
  • Biotinidase Deficiency
  • Bloom Syndrome
  • Canavan Disease
  • 21-hydroxylase Deficient Congenital Adrenal Hyperplasia
  • Familial Dysautonomia
  • Fanconi Anemia Type C
  • Gaucher Disease
  • Glycogen Storage Disease Type Ia
  • Hb Beta Chain-related Hemoglobinopathy (including Beta Thalassemia And Sickle Cell Disease)
  • Hexosaminidase A Deficiency (including Tay-Sachs Disease)
  • Joubert Syndrome 2
  • Maple Syrup Urine Disease Type 1B
  • Mucolipidosis IV
  • NEB-related Nemaline Myopathy
  • Niemann-Pick Disease, SMPD1-associated
  • Usher Syndrome Type 1F
  • Usher Syndrome Type 3
  • Walker-Warburg Syndrome
  • 11-beta-hydroxylase-deficient Congenital Adrenal Hyperplasia
  • Bernard-Soulier Syndrome, Type C
  • Congenital Amegakaryocytic Thrombocytopenia (MPL)
  • Deafness, Autosomal Recessive 9 / Auditory Neuropathy