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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NBN
(Q344* +1 more)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic/Likely pathogenic
NBN
(L281* +1 more)
Single nucleotide variant
(nonsense)
Aplastic anemia
+3 more
GPathogenic