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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTLA4
(R70W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
CTLA4
(Q76*)
Single nucleotide variant
(nonsense)
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
GPathogenic
CTLA4
(P158S)
Single nucleotide variant
(missense variant +1 more)
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
GUncertain significance
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