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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARFGEF2
(R196C)
Single nucleotide variant
(missense variant)
Periventricular heterotopia with microcephaly, autosomal recessive
+1 more
GUncertain significance
ARFGEF2
(R925* +1 more)
Single nucleotide variant
(nonsense)
Periventricular heterotopia with microcephaly, autosomal recessive
GUncertain significance
ARFGEF2
(R1756W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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