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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRRC8A
(L756fs)
Deletion
(frameshift variant)
Agammaglobulinemia 5, autosomal dominant
GUncertain significance
ABL1, AIF1L
+38 more
Copy number loss
not provided
GLikely pathogenic