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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT1
(N188K)
Single nucleotide variant
(missense variant)
KRT1-related disorder
+2 more
GPathogenic
KRT10, KRT10-AS1
(S33F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance