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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NBN
(K137fs +1 more)
Deletion
(frameshift variant)
Microcephaly
+6 more
GPathogenic
NBN
(I171V +1 more)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+9 more
GConflicting classifications of pathogenicity