RS398122394 ALG13

Health Risk Chr X:111685040
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
36
Rare genetic intellectual disability
Seizure
Intellectual disability
Hypotonia
Microcephaly
Neurodevelopmental delay
Inborn genetic diseases
ALG13-related disorder
Developmental and epileptic encephalopathy
36
Developmental and epileptic encephalopathy
36
Rare genetic intellectual disability
Other Variants in ALG13
rs867599353 rs750710267 rs190790872 rs781178409 rs374174400 rs756238772 rs56717389 rs372521943 rs774331771 rs747478031
Ask Dr. Hemsworth about this variant