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Links from MedGen

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT10, KRT10-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
Epidermolytic hyperkeratosis 2A, autosomal dominant
+1 more
GLikely pathogenic
KRT10, KRT10-AS1
(R156L)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 2A, autosomal dominant
GPathogenic
KRT10, KRT10-AS1
(M150T)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
KRT10-AS1, KRT10
(M150R)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 2A, autosomal dominant
GPathogenic
KRT10, KRT10-AS1
(R156C)
Single nucleotide variant
(missense variant)
Epidermolytic nevus
+5 more
GPathogenic
KRT10, KRT10-AS1
(L442Q)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 2A, autosomal dominant
GPathogenic
KRT10, KRT10-AS1
(R156H)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 2A, autosomal dominant
+2 more
GPathogenic
KRT10, KRT10-AS1
(Y160D)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 2A, autosomal dominant
GPathogenic
KRT10, KRT10-AS1
(N154H)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 2A, autosomal dominant
GPathogenic
KRT10, KRT10-AS1
(L161S)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 2A, autosomal dominant
GPathogenic
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