"Mendelics"[submitter] AND "EDNRB"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1684703	NM_001122659.3(EDNRB):c.928G>A (p.Ala310Thr)	EDNRB, EDNRB-AS1 (A310T +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 225346	NM_001122659.3(EDNRB):c.-26G>A	EDNRB (R82Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity