RS201253231 RTTN

Health Risk Chr 18:70017527
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
RTTN-related disorder
Inborn genetic diseases
RTTN-related disorder
Other Variants in RTTN
rs318240757 rs143471549 rs199597732 rs34989098 rs797044691 rs35313369 rs200600259 rs780270096 rs864321621 rs864321620
Ask Dr. Hemsworth about this variant