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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRIT1
(A410T +2 more)
Single nucleotide variant
(missense variant)
Cerebral cavernous malformation
GUncertain significance
KRIT1
(P357S +2 more)
Single nucleotide variant
(missense variant)
Cerebral cavernous malformation
GUncertain significance
KRIT1
Single nucleotide variant
(intron variant)
not provided
+1 more
GLikely pathogenic
KRIT1
(R49fs)
Microsatellite
(frameshift variant +1 more)
Cerebral cavernous malformation
GPathogenic/Likely pathogenic
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