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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTRC
(S16I)
Single nucleotide variant
(missense variant)
Hereditary pancreatitis
GUncertain significance
CTRC
Single nucleotide variant
(splice acceptor variant)
Hereditary pancreatitis
GPathogenic/Likely pathogenic
CTRC
(G217S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CTRC
Deletion
(inframe_deletion)
not specified
+2 more
GPathogenic
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