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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRF1
(P22L)
Single nucleotide variant
(missense variant)
Familial hemophagocytic lymphohistiocytosis 2
+2 more
GUncertain significance
PRF1
(R4C)
Single nucleotide variant
(missense variant)
Aplastic anemia
+4 more
GConflicting classifications of pathogenicity