Chain1182: Nonspecific Cardiac Conduction Defect
This is a rare disease.
Example use A
Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.
Developer
Dr. Colby
Genetic info
Genes | Genetic variants |
---|---|
SCN1B | chr19:35524454,chr19:35524732 |