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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXW4, LOC130004563
Single nucleotide variant
(synonymous variant +2 more)
not provided
+1 more
GLikely benign
FBXW4, LOC130004563
(G153R)
Single nucleotide variant
(missense variant +2 more)
FBXW4-related condition
+1 more
GConflicting classifications of pathogenicity