RS764595221 SPEN

Health Risk Chr 1:15928646
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Associated Conditions
Neurodevelopmental abnormality
Radio-Tartaglia syndrome
Inborn genetic diseases
Neurodevelopmental abnormality
Radio-Tartaglia syndrome
Inborn genetic diseases
Other Variants in SPEN
rs751475729 rs150756182 rs2071205857 rs2071207771 rs2071236139 rs2071239657 rs2071226510 rs2148733237 rs2148737783 rs2148737840
Ask Dr. Hemsworth about this variant