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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP27A1
(T339M)
Single nucleotide variant
(missense variant)
Cholestanol storage disease
+1 more
GPathogenic/Likely pathogenic
CYP27A1
(R405Q)
Single nucleotide variant
(missense variant)
Cholestanol storage disease
+1 more
GPathogenic/Likely pathogenic
CYP27A1
(G472A)
Single nucleotide variant
(missense variant)
Cholestanol storage disease
GPathogenic/Likely pathogenic
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