List of variants in gene DCN reported as benign for corneal disorder

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001920.5(DCN):c.*51A>G	rs1803343	0.02082
NM_001920.5(DCN):c.282C>T (p.Thr94=)	rs3138221	0.01829
NM_001920.5(DCN):c.803C>T (p.Thr268Met)	rs3138268	0.01757
NM_001920.5(DCN):c.424A>G (p.Lys142Glu)	rs142752401	0.00605
NM_001920.5(DCN):c.703A>C (p.Arg235=)	rs3138264	0.00551
NM_001920.5(DCN):c.917T>C (p.Val306Ala)	rs73358055	0.00491
NM_001920.5(DCN):c.33A>G (p.Ala11=)	rs141738168	0.00477
NM_001920.5(DCN):c.975G>A (p.Ser325=)	rs80123678	0.00454
NM_001920.5(DCN):c.212-6T>C	rs191218249	0.00230
NM_001920.5(DCN):c.529A>T (p.Ile177Phe)	rs201430261	0.00016
NM_001920.5(DCN):c.671C>T (p.Thr224Met)	rs144174426	0.00012
NM_001920.5(DCN):c.*105G>A	rs191434778	0.00010
NM_001920.5(DCN):c.*160C>T	rs7441
NM_001920.5(DCN):c.*377T>C	rs35379812

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