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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SNCA
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+1 more
GUncertain significance
SNCA
(A53V)
Single nucleotide variant
(non-coding transcript variant +1 more)
Autosomal dominant Parkinson disease 1
+2 more
GUncertain significance