List of variants in gene EDN3 reported as likely pathogenic for intestinal motility disease

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_207034.3(EDN3):c.293C>A (p.Thr98Lys)	rs745795470	0.00002
NM_207034.3(EDN3):c.332G>T (p.Cys111Phe)	rs773779627
NM_207034.3(EDN3):c.334C>A (p.His112Asn)	rs977075341
NM_207034.3(EDN3):c.565dup (p.Thr189fs)	rs11570344

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