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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1A
(D1697G +1 more)
Single nucleotide variant
(missense variant)
Microcephaly
+7 more
GConflicting classifications of pathogenicity
ARID1A
(E2036del +1 more)
Microsatellite
(inframe_deletion)
Intellectual disability, autosomal dominant 14
GUncertain significance