List of variants in gene EVC reported as benign for not specified

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: 41

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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.2894+18A>G	rs2279250	0.71871
NM_153717.3(EVC):c.939+10A>G	rs2286342	0.67122
NM_153717.3(EVC):c.*14G>A	rs2291151	0.61437
NM_153717.3(EVC):c.802-15C>T	rs4689313	0.60798
NM_153717.3(EVC):c.1026G>C (p.Leu342=)	rs4688962	0.52761
NM_153717.3(EVC):c.969T>C (p.Asn323=)	rs4688963	0.40746
NM_153717.3(EVC):c.1099-19T>C	rs899691	0.37351
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.2305-44C>T	rs2306400	0.26578
NM_153717.3(EVC):c.1465-47A>C	rs4642178	0.20086
NM_153717.3(EVC):c.174+31G>C	rs2276874	0.14512
NM_153717.3(EVC):c.249A>G (p.Ser83=)	rs35870680	0.09998
NM_153717.3(EVC):c.384+41C>T	rs113870218	0.08516
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.939+11G>T	rs55955937	0.02788
NM_153717.3(EVC):c.2279G>A (p.Arg760Gln)	rs2279252	0.01416
NM_153717.3(EVC):c.1464+8A>G	rs116236414	0.01163
NM_153717.3(EVC):c.385-16C>T	rs113571700	0.00995
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.284A>G (p.Asp95Gly)	rs41269547	0.00561
NM_153717.3(EVC):c.1855G>A (p.Val619Ile)	rs111293777	0.00354
NM_153717.3(EVC):c.1127C>T (p.Ala376Val)	rs142535134	0.00309
NM_153717.3(EVC):c.934G>A (p.Asp312Asn)	rs115275195	0.00171
NM_153717.3(EVC):c.1333A>C (p.Lys445Gln)	rs116952023	0.00150
NM_153717.3(EVC):c.473C>G (p.Ser158Cys)	rs150284356	0.00011
NM_153717.3(EVC):c.1346C>A (p.Thr449Lys)	rs2302075
NM_153717.3(EVC):c.1528G>A (p.Val510Ile)	rs143971158
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.2562-4C>G	rs60082311
NM_153717.3(EVC):c.802-17TTC[4]	rs370315662

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