Chain1321: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions
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 |
---|---|
PEO1 | chr10:102749073 |
POLG | chr15:89873415,chr15:89873415,chr15:89872286,chr15:89870432,chr15:89868870,chr15:89868870 |