Chain136: Albinism, Oculocutaneous, Type III
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 |
---|---|
TYRP1 | chr9:12705626,chr9:12714564,chr9:12712424,chr9:12714547,chr9:12704103,chr9:12712414 |