RS786205208 NEXMIF

Health Risk Chr X:74742675
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What This Variant Does
"CLNSIG=4
Associated Conditions
X-linked intellectual disability
Cantagrel type
Inborn genetic diseases
Seizure
X-linked intellectual disability
Cantagrel type
Inborn genetic diseases
Seizure
Other Variants in NEXMIF
rs397518478 rs397518479 rs186535459 rs727503977 rs751468762 rs797045646 rs764439412 rs875989829 rs758719615 rs878854425
Ask Dr. Hemsworth about this variant