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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDCD10
(Y181C)
Single nucleotide variant
(missense variant)
Cerebral cavernous malformation 3
GUncertain significance
PDCD10
Single nucleotide variant
(intron variant)
Cerebral cavernous malformation 3
+6 more
GPathogenic/Likely pathogenic
PDCD10
(Y23fs)
Deletion
(frameshift variant)
Cerebral cavernous malformation 3
GPathogenic
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