Chain1158: Neuropathy, Hereditary Sensory, Type I
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 |
---|---|
SPTLC1 | chr9:94842326,chr9:94830377 |