List of variants reported as likely pathogenic for Jeune syndrome by Natera, Inc.

Minimum submission review status:		Collection method:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.2782+1G>T	rs1007534611	0.00002
NM_153717.3(EVC):c.901AAG[1] (p.Lys302del)	rs755381180
NM_153717.3(EVC):c.939+1G>A	rs1553873138

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