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

GenesGenetic variants
SLC14A1chr18:45060240,chr18:45062615

Qualitative

Type

text

Possible responses

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