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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF9
(I402V +10 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GLikely benign
ARHGEF9
(S141G +7 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 8
GUncertain significance