List of variants in gene EVC reported as benign by Natera, Inc.

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.769C>T (p.Leu257=)	rs6446393	0.95639
NM_153717.3(EVC):c.2305-8T>C	rs1031919	0.72106
NM_153717.3(EVC):c.772T>C (p.Tyr258His)	rs6414624	0.72068
NM_153717.3(EVC):c.939+10A>G	rs2286342	0.67122
NM_153717.3(EVC):c.1026G>C (p.Leu342=)	rs4688962	0.52761
NM_153717.3(EVC):c.939+4C>T	rs2286343	0.33466
NM_153717.3(EVC):c.1068A>G (p.Leu356=)	rs33929747	0.26691
NM_153717.3(EVC):c.249A>G (p.Ser83=)	rs35870680	0.09998
NM_153717.3(EVC):c.221A>C (p.Gln74Pro)	rs2291157	0.07908
NM_153717.3(EVC):c.1328G>A (p.Arg443Gln)	rs35953626	0.07232
NM_153717.3(EVC):c.1115C>T (p.Thr372Met)	rs28483498	0.06438
NM_153717.3(EVC):c.341C>T (p.Ala114Val)	rs16837598	0.05943
NM_153717.3(EVC):c.1096C>T (p.Leu366=)	rs6854138	0.03243
NM_153717.3(EVC):c.1464+8A>G	rs116236414	0.01163
NM_153717.3(EVC):c.2373G>A (p.Gln791=)	rs73795089	0.01161
NM_153717.3(EVC):c.2363G>A (p.Arg788His)	rs73795088	0.01159
NM_153717.3(EVC):c.2872G>A (p.Asp958Asn)	rs35287723	0.00977
NM_153717.3(EVC):c.2505G>A (p.Ser835=)	rs115976359	0.00969
NM_153717.3(EVC):c.1320T>A (p.Phe440Leu)	rs60582583	0.00733
NM_153717.3(EVC):c.780G>A (p.Lys260=)	rs41269555	0.00676
NM_153717.3(EVC):c.469C>G (p.Pro157Ala)	rs146729456	0.00451
NM_153717.3(EVC):c.1855G>A (p.Val619Ile)	rs111293777	0.00354
NM_153717.3(EVC):c.939+9C>T	rs201282320	0.00205
NM_153717.3(EVC):c.1369G>A (p.Glu457Lys)	rs141859946	0.00188
NM_153717.3(EVC):c.1333A>C (p.Lys445Gln)	rs116952023	0.00150
NM_153717.3(EVC):c.1346C>A (p.Thr449Lys)	rs2302075
NM_153717.3(EVC):c.1727G>A (p.Arg576Gln)	rs1383180
NM_153717.3(EVC):c.1854C>T (p.Gly618=)	rs11737221
NM_153717.3(EVC):c.2449+15del	rs398092136
NM_153717.3(EVC):c.2562-4C>G	rs60082311

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