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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRSS12
(R797C)
Single nucleotide variant
(missense variant)
not specified
+2 more
GLikely benign
PRSS12
(Q710fs)
Duplication
(frameshift variant)
not specified
+1 more
GUncertain significance
PRSS12
Single nucleotide variant
(splice acceptor variant)
not specified
+1 more
GUncertain significance
PRSS12
(G175S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
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