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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRSS1, TRB
(N29I)
Single nucleotide variant
(missense variant)
Trypsinogen deficiency
+3 more
GPathogenic
PRSS1, TRB
(P36R)
Single nucleotide variant
(missense variant)
Hereditary pancreatitis
+1 more
GUncertain significance
PRSS1, TRB
(I93F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TRB, PRSS1
(R116H)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
PRSS1, TRB
(R122H)
Single nucleotide variant
(missense variant)
PRSS1-related condition
+2 more
GPathogenic
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