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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EDA
(R69L)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
EDA
(R153H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
EDA
Deletion
(intron variant)
Hypohidrotic X-linked ectodermal dysplasia
+2 more
GBenign
EDA
Single nucleotide variant
(intron variant)
Hypohidrotic X-linked ectodermal dysplasia
+2 more
GBenign
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