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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRIT1
(R423* +2 more)
Single nucleotide variant
(nonsense)
KRIT1-related disorder
+2 more
GPathogenic
KRIT1
(Y327* +1 more)
Single nucleotide variant
(nonsense +1 more)
Cerebral cavernous malformation
GLikely pathogenic
KRIT1
(W271* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
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