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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCM2, LOC129998395
Indel
(intron variant)
not provided
+1 more
GPathogenic/Likely pathogenic
ARMC10, ASB4
+504 more
Inversion
Childhood apraxia of speech
GPathogenic
CCM2
Deletion
Cerebral cavernous malformation 2
GPathogenic
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