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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WRAP53
(V302F)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GPathogenic
WRAP53
(R398W)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity