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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXO7
Single nucleotide variant
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
FBXO7
(M115I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign
FBXO7
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GConflicting classifications of pathogenicity
FBXO7
(V485I +2 more)
Single nucleotide variant
(missense variant)
Parkinsonian-pyramidal syndrome
+1 more
GUncertain significance
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