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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EDAR, RANBP2
Single nucleotide variant
(splice donor variant)
Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
GPathogenic
EDAR, RANBP2
(C113Y)
Single nucleotide variant
(missense variant)
Oligodontia
GPathogenic