RS864321621 RTTN

Health Risk Chr 18:70127695
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Primary microcephaly
Microcephalic primordial dwarfism due to RTTN deficiency
Primary microcephaly
Microcephalic primordial dwarfism due to RTTN deficiency
Other Variants in RTTN
rs318240757 rs143471549 rs199597732 rs34989098 rs797044691 rs35313369 rs200600259 rs780270096 rs864321620 rs775277800
Ask Dr. Hemsworth about this variant