Chain643: Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
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 |
---|---|
PRKAG2 | chr7:151265836,chr7:151265887,chr7:151261285,chr7:151269750 |