RS34989098 RTTN

Health Risk Chr 18:70006461
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Associated Conditions
Microcephalic primordial dwarfism due to RTTN deficiency
RTTN-related disorder
Inborn genetic diseases
Microcephalic primordial dwarfism due to RTTN deficiency
RTTN-related disorder
Inborn genetic diseases
Other Variants in RTTN
rs318240757 rs143471549 rs199597732 rs797044691 rs35313369 rs200600259 rs780270096 rs864321621 rs864321620 rs775277800
Ask Dr. Hemsworth about this variant