List of variants in gene OCLN reported as likely pathogenic by GeneDx

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001205254.2(OCLN):c.724C>T (p.Gln242Ter)	rs1472215562	0.00001
NM_001205254.2(OCLN):c.1218C>T (p.Gly406=)	rs767324023
NM_001205254.2(OCLN):c.23del (p.Ser8fs)	rs1580547770

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