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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFI
(A511V +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GUncertain significance
CFI
(K441R +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+7 more
GConflicting classifications of pathogenicity