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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EDAR, RANBP2
(C428*)
Single nucleotide variant
(nonsense)
Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
GLikely pathogenic
EDAR, RANBP2
(R89H)
Single nucleotide variant
(missense variant)
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
+1 more
GPathogenic
EDAR, RANBP2
(R89C)
Single nucleotide variant
(missense variant)
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
+1 more
GPathogenic
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