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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NBN
Single nucleotide variant
(splice donor variant)
Aplastic anemia
+3 more
GLikely pathogenic
NBN
(K137fs +1 more)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+6 more
GPathogenic
NBN
(S113N +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
NBN
Single nucleotide variant
(splice donor variant)
Microcephaly, normal intelligence and immunodeficiency
+4 more
GPathogenic/Likely pathogenic
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