List of variants in gene EVC reported as likely benign by Illumina Laboratory Services, Illumina

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: 25

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HGVS	dbSNP	gnomAD frequency
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.*2126T>G	rs191415414	0.00444
NM_153717.3(EVC):c.1127C>T (p.Ala376Val)	rs142535134	0.00309
NM_153717.3(EVC):c.*491C>T	rs114993332	0.00287
NM_153717.3(EVC):c.*2692G>T	rs149155153	0.00279
NM_153717.3(EVC):c.532G>A (p.Val178Ile)	rs144897690	0.00243
NM_153717.3(EVC):c.1636A>G (p.Met546Val)	rs112608085	0.00209
NM_153717.3(EVC):c.550G>A (p.Asp184Asn)	rs41269549	0.00194
NM_153717.3(EVC):c.1369G>A (p.Glu457Lys)	rs141859946	0.00188
NM_153717.3(EVC):c.934G>A (p.Asp312Asn)	rs115275195	0.00171
NM_153717.3(EVC):c.*2493A>G	rs188345323	0.00114
NM_153717.3(EVC):c.*492G>A	rs530991301	0.00090
NM_153717.3(EVC):c.*994C>T	rs547970729	0.00071
NM_153717.3(EVC):c.*2310G>A	rs539844915	0.00041
NM_153717.3(EVC):c.1995G>A (p.Ser665=)	rs142897994	0.00038
NM_153717.3(EVC):c.*2125T>G	rs139771274	0.00033
NM_153717.3(EVC):c.2276G>A (p.Ser759Asn)	rs201776972	0.00025
NM_153717.3(EVC):c.2241G>A (p.Ala747=)	rs142094016	0.00014
NM_153717.3(EVC):c.982C>T (p.Leu328Phe)	rs199916502	0.00011
NM_153717.3(EVC):c.1564-6C>T	rs188245524	0.00008
NM_153717.3(EVC):c.1313G>A (p.Arg438Gln)	rs373718642	0.00002
NM_153717.3(EVC):c.*1314G>A	rs567979829
NM_153717.3(EVC):c.*1439C>T	rs188270163
NM_153717.3(EVC):c.2895-10_2895-9del	rs371125826

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