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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP4F22
(F59L)
Single nucleotide variant
(missense variant)
Lamellar ichthyosis
+2 more
GPathogenic/Likely pathogenic
CYP4F22
(R154Q)
Single nucleotide variant
(missense variant)
Autosomal recessive congenital ichthyosis 5
GUncertain significance
CYP4F22
(R157H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CYP4F22
(H435Y)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
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