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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADGRG1
(P346A +7 more)
Single nucleotide variant
(missense variant)
Polymicrogyria, bilateral perisylvian, autosomal recessive
+1 more
GUncertain significance
ADGRG1
(S467F +7 more)
Single nucleotide variant
(missense variant)
Bilateral frontoparietal polymicrogyria
GLikely pathogenic