List of variants in gene DSE reported as benign for cardiovascular 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_013352.4(DSE):c.1926T>C (p.Asn642=)	rs560644	0.95438
NM_013352.4(DSE):c.74C>T (p.Thr25Ile)	rs10485183	0.23388
NM_013352.4(DSE):c.1142T>C (p.Val381Ala)	rs41313440	0.05356
NM_013352.4(DSE):c.1926= (p.Asn642=)	rs560644	0.04562
NM_013352.4(DSE):c.101C>T (p.Pro34Leu)	rs35548455	0.04141
NM_013352.4(DSE):c.53G>T (p.Cys18Phe)	rs76186865	0.03160
NM_013352.4(DSE):c.844A>G (p.Ile282Val)	rs34994230	0.02817
NM_013352.4(DSE):c.1118+15G>A	rs116330739	0.01381
NM_013352.4(DSE):c.114C>T (p.Ala38=)	rs36061922	0.00553
NM_013352.4(DSE):c.711G>C (p.Leu237=)	rs140034597	0.00484
NM_013352.4(DSE):c.209G>A (p.Arg70His)	rs147683614	0.00278
NM_013352.4(DSE):c.216G>A (p.Thr72=)	rs61747210	0.00164
NM_013352.4(DSE):c.2334G>T (p.Leu778=)	rs534248134	0.00001
NM_013352.4(DSE):c.2619_2621del (p.Gly874del)	rs111252008

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