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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT1
(V623fs)
Duplication
(frameshift variant)
Congenital reticular ichthyosiform erythroderma
GPathogenic
KRT10, KRT10-AS1
(R156C)
Single nucleotide variant
(missense variant)
KRT10-related disorder
+5 more
GPathogenic