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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPCAM
(Q89H)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
EPCAM
(G103R)
Single nucleotide variant
(missense variant)
not provided
GPathogenic/Likely pathogenic
EPCAM
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
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