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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOLR1
(R98W)
Single nucleotide variant
(missense variant)
Cerebral folate transport deficiency
+3 more
GBenign/Likely benign
FOLR1
(A170T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity