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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRNP
(H69L)
Single nucleotide variant
(missense variant +1 more)
Gerstmann-Straussler-Scheinker syndrome
GUncertain significance
PRNP
(D178N)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic
PRNP
(V180I)
Single nucleotide variant
(missense variant +1 more)
Gerstmann-Straussler-Scheinker syndrome
+6 more
GPathogenic/Likely pathogenic/Pathogenic, low penetrance
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