List of variants in gene EVC reported as likely 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: 21

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.2505G>A (p.Ser835=)	rs115976359	0.00969
NM_153717.3(EVC):c.284A>G (p.Asp95Gly)	rs41269547	0.00561
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.1127C>T (p.Ala376Val)	rs142535134	0.00309
NM_153717.3(EVC):c.1636A>G (p.Met546Val)	rs112608085	0.00209
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.1040C>T (p.Thr347Met)	rs34947207	0.00127
NM_153717.3(EVC):c.2712C>T (p.Ser904=)	rs146829332	0.00034
NM_153717.3(EVC):c.2298C>T (p.Asp766=)	rs140546984	0.00011
NM_153717.3(EVC):c.2895-4T>C	rs775049818	0.00008
NM_153717.3(EVC):c.1692C>T (p.Asn564=)	rs138242443	0.00006
NM_153717.3(EVC):c.1018C>A (p.Arg340=)	rs121908425
NM_153717.3(EVC):c.1041G>T (p.Thr347=)	rs148418233
NM_153717.3(EVC):c.1098+12G>C
NM_153717.3(EVC):c.1464+20T>C	rs886038740
NM_153717.3(EVC):c.2449+15del	rs398092136
NM_153717.3(EVC):c.801+13C>T	rs545838582
NM_153717.3(EVC):c.930A>G (p.Leu310=)	rs776792609
NM_153717.3(EVC):c.945A>G (p.Glu315=)	rs1057523442

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