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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADRM1, ARFGAP1
+198 more
Duplication
not specified
GUncertain significance
CDH4
(E451K +2 more)
Single nucleotide variant
(missense variant)
Simplified gyral pattern
GUncertain significance
CDH4
(R659P +2 more)
Single nucleotide variant
(missense variant)
Abnormal brain morphology
GLikely pathogenic
CDH4
(A852T +2 more)
Single nucleotide variant
(missense variant)
Simplified gyral pattern
GUncertain significance
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