Chain1569: Usher Syndrome, Type 1b
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 |
---|---|
MYO7A | chr11:76867949,chr11:76885862,chr11:76869378,chr11:76900388 |