List of variants in gene DCN reported as not provided for corneal disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001920.5(DCN):c.1036T>G (p.Cys346Gly)
NM_001920.5(DCN):c.941del (p.Pro314fs)	rs80338742
NM_001920.5(DCN):c.947del (p.Gly316fs)	rs397515545
NM_001920.5(DCN):c.962del (p.Lys321fs)	rs587777258
NM_001920.5(DCN):c.967del (p.Ser323fs)	rs80338741

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