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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHCR7
(W151*)
Single nucleotide variant
(nonsense)
DHCR7-related disorder
+7 more
GPathogenic/Likely pathogenic
RAB11A
(H112R)
Single nucleotide variant
(missense variant)
Intellectual disability, mild
+6 more
GLikely pathogenic