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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCF3
(P529R +1 more)
Single nucleotide variant
(missense variant +1 more)
Agammaglobulinemia 8, autosomal dominant
+1 more
GUncertain significance
TCF3
(S445fs +1 more)
Deletion
(frameshift variant)
Agammaglobulinemia 8, autosomal dominant
GLikely pathogenic