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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARX
(P403fs)
Deletion
(frameshift variant)
X-linked lissencephaly with abnormal genitalia
GLikely pathogenic
ARX
(R358K)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 1
GUncertain significance
ARX, LOC109610631
Microsatellite
(inframe_insertion)
Developmental and epileptic encephalopathy, 1
+5 more
GPathogenic/Likely pathogenic
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