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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PINK1, PINK1-AS
(M318L)
Single nucleotide variant
(missense variant)
Autosomal recessive early-onset Parkinson disease 6
+2 more
GUncertain significance
PINK1-AS, PINK1
(R492*)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GPathogenic