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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GDF6
(K424R)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis 17
+4 more
GConflicting classifications of pathogenicity
LRRK2
(R1628P)
Single nucleotide variant
(missense variant)
Parkinson disease
+2 more
GConflicting classifications of pathogenicity