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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PINK1, PINK1-AS
Single nucleotide variant
(synonymous variant)
Autosomal recessive early-onset Parkinson disease 6
+1 more
GConflicting classifications of pathogenicity
PINK1, PINK1-AS
(M318L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
PINK1, PINK1-AS
(A339T)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
PINK1, PINK1-AS
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
PINK1, PINK1-AS
(E476K)
Single nucleotide variant
(non-coding transcript variant +1 more)
PINK1-related condition
+3 more
GBenign/Likely benign
DDOST, PINK1
+1 more
(N521T)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+4 more
GBenign/Likely benign
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