RS2080101661 NEXMIF

Health Risk Chr X:74741132
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Associated Conditions
Inborn genetic diseases
X-linked intellectual disability
Cantagrel type
Inborn genetic diseases
X-linked intellectual disability
Cantagrel type
Other Variants in NEXMIF
rs397518478 rs397518479 rs186535459 rs727503977 rs786205208 rs751468762 rs797045646 rs764439412 rs875989829 rs758719615
Ask Dr. Hemsworth about this variant