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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRNP
(S39P)
Single nucleotide variant
(synonymous variant +1 more)
Huntington disease-like 1
+2 more
GBenign
PRNP
Single nucleotide variant
(synonymous variant +1 more)
Huntington disease-like 1
+2 more
GBenign
PRNP
Single nucleotide variant
(synonymous variant +1 more)
Inherited prion disease
+2 more
GBenign/Likely benign
PRNP
(M129V)
Single nucleotide variant
(missense variant +1 more)
not provided
+7 more
GBenign/Likely benign
PRNP
(N171S)
Single nucleotide variant
(missense variant +1 more)
Inherited prion disease
+2 more
GBenign
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