RS201473797 RTTN

Health Risk Chr 18:70073944
Upload your DNA to see your genotype for this variant.
Associated Conditions
Microcephalic primordial dwarfism due to RTTN deficiency
Inborn genetic diseases
Microcephalic primordial dwarfism due to RTTN deficiency
Inborn genetic diseases
Other Variants in RTTN
rs318240757 rs143471549 rs199597732 rs34989098 rs797044691 rs35313369 rs200600259 rs780270096 rs864321621 rs864321620
Ask Dr. Hemsworth about this variant