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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT9
(Y167S)
Single nucleotide variant
(missense variant)
Epidermolytic palmoplantar keratoderma
GLikely pathogenic
KRT9
(R163Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GPathogenic/Likely pathogenic
KRT9
(N161K)
Single nucleotide variant
(missense variant)
Epidermolytic palmoplantar keratoderma
GLikely pathogenic
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