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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLE
(L2274V)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
POLE
(A427V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance