"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "EDN3"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 339115	NM_207034.2(EDN3):c.-248G>A	EDN3	Single nucleotide variant	not specified +2 more	GBenign/Likely benign
Select item 16646	NM_207034.3(EDN3):c.49G>A (p.Ala17Thr)	EDN3 (A17T)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1335463	NM_207034.3(EDN3):c.589-10C>T	EDN3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign

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