Chain412: Congenital Myasthenic Syndrome associated with Acetylcholine Receptor Deficiency
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 |
---|---|
RAPSN | chr11:47470726,chr11:47469631 |