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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP7B1
(R486C)
Single nucleotide variant
(missense variant +1 more)
Hereditary spastic paraplegia 5A
+4 more
GPathogenic/Likely pathogenic
CYP7B1
(T177M)
Single nucleotide variant
(missense variant)
Congenital bile acid synthesis defect 3
+3 more
GConflicting classifications of pathogenicity