ClinVar Miner

List of variants in gene EDN3 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_207034.3(EDN3):c.-19C>A	rs375594972	0.00009
NM_207034.3(EDN3):c.-86G>A	rs755284881	0.00008

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