ClinVar (all) for Orgtrack (Select 507617) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 972718	NM_022336.4(EDAR):c.287T>C (p.Phe96Ser)	EDAR, RANBP2 (F96S)	Single nucleotide variant (missense variant)	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant	GLikely pathogenic
Select item 228257	NM_001399.5(EDA):c.866G>A (p.Arg289His)	EDA (R289H +1 more)	Single nucleotide variant (missense variant)	Partial congenital absence of teeth +4 more	GPathogenic/Likely pathogenic