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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRKN
(P437L +2 more)
Single nucleotide variant
(missense variant)
Autosomal recessive juvenile Parkinson disease 2
+1 more
GConflicting classifications of pathogenicity
PRKN
(D394N +2 more)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+4 more
GBenign/Likely benign
PRKN
(V380L +2 more)
Single nucleotide variant
(missense variant)
Autosomal recessive juvenile Parkinson disease 2
+4 more
GBenign
PRKN
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
PRKN
(R334C +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PRKN
(M192L)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GBenign
PRKN
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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