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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPCAM
(Q45L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
EPCAM
(T113I)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
EPCAM
(M308L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
EPCAM, MSH2
Deletion
Hereditary cancer-predisposing syndrome
GPathogenic
EPCAM, MSH2
Deletion
Hereditary cancer-predisposing syndrome
GPathogenic
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