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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDC73
Duplication
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
CDC73
Indel
(intron variant)
not provided
GUncertain significance
CDC73
Single nucleotide variant
(splice donor variant)
not provided
GPathogenic
CDC73
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
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