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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTLA4
(V40M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely pathogenic
CTLA4
(A54T)
Single nucleotide variant
(missense variant)
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
GConflicting classifications of pathogenicity