Chain398: Congenital disorders of glycosylation type 1G
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 |
---|---|
ALG12 | chr22:50304114,chr22:50301430 |