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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRIT1
(Q407* +2 more)
Single nucleotide variant
(nonsense)
Cerebral cavernous malformation
+3 more
GPathogenic
NOTCH3
(T987S)
Single nucleotide variant
(missense variant)
Myofibromatosis, infantile, 2
+3 more
GConflicting classifications of pathogenicity