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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP4F22
(R243H)
Single nucleotide variant
(missense variant)
Lamellar ichthyosis
+1 more
GPathogenic
CYP4F22
(R372W)
Single nucleotide variant
(missense variant)
Autosomal recessive congenital ichthyosis 5
GLikely pathogenic