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

GenesGenetic variants
TYRP1chr9:12705626,chr9:12714564,chr9:12712424,chr9:12714547,chr9:12704103,chr9:12712414

Qualitative

Type

text

Possible responses

Carrier, Possibly Affected, Not Detected, insufficient data, error