Chain1567: Urea Transport Defect JK-Null Variant
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 |
---|---|
SLC14A1 | chr18:45060240,chr18:45062615 |