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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CISD3, PCGF2
(G221R)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+1 more
GUncertain significance
PCGF2
(P65L)
Single nucleotide variant
(missense variant)
Intellectual disability
+4 more
GPathogenic/Likely pathogenic