| Table 1. Comparison of carrier frequencies for top 10 disorders observed in each panel | |||||
| Panel A | Panel B | Panel C | |||
| Disorder | Carriers | Disorder | Carriers | Disorder | Carriers |
| GJB2-Related Nonsyndromic hearing loss and deafness | 26 | Familial Mediterranean Fever | 14 | Alpha-1 antitrypsin deficiency | 14 |
| Biotinidase Deficiency | 19 | CFTR-Related disorders | 14 | 21-hydroxylase deficiency | 11 |
| Cystic Fibrosis | 11 | Wilson disease | 14 | Alpha thalassemia | 8 |
| Familial Mediterranean Fever | 10 | GJB2-Related Nonsyndromic hearing loss and deafness | 7 | CFTR-Related disorders | 7 |
| Pseudocholinesterase Deficiency | 10 | SMN1 Linked Spinal Muscular Atrophy | 7 | Familial Mediterranean Fever | 7 |
| SMN1 Linked Spinal Muscular Atrophy | 8 | Progressive familial intrahepatic cholestasis | 7 | Tyrosinemia type I | 7 |
| Hereditary Fructose Intolerance | 6 | Primary coenzyme Q10 deficiency | 7 | Oculocutaneous albinism type II | 5 |
| Type I Glutaric Acidemia | 6 | Muscular dystrophy-dystroglycanopathy type C3 | 7 | SMN1 Linked Spinal Muscular Atrophy | 5 |
| Classical Galactosemia | 5 | Cystic Fibrosis | 6 | Glucose-6-phosphate dehydrogenase deficiency | 5 |
| Glycogen Storage Disease: Type II | 5 | Classical Galactosemia | 6 | GJB2-Related Nonsyndromic hearing loss and deafness | 4 |