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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFI
(E548Q +4 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+3 more
GConflicting classifications of pathogenicity
CFI
(G119R)
Single nucleotide variant
(missense variant +2 more)
not specified
+3 more
GConflicting classifications of pathogenicity
CFI
(A76G)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
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