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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP27A1
(P146L)
Single nucleotide variant
(missense variant)
Cholestanol storage disease
GUncertain significance
CYP27A1
(R395C)
Single nucleotide variant
(missense variant)
CYP27A1-related condition
+2 more
GPathogenic/Likely pathogenic