Variants in gene EVC with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 17

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.1328G>A (p.Arg443Gln)	rs35953626	0.07232
NM_153717.3(EVC):c.2279G>A (p.Arg760Gln)	rs2279252	0.01416
NM_153717.3(EVC):c.2363G>A (p.Arg788His)	rs73795088	0.01159
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.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.532G>A (p.Val178Ile)	rs144897690	0.00243
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.934G>A (p.Asp312Asn)	rs115275195	0.00171
NM_153717.3(EVC):c.1333A>C (p.Lys445Gln)	rs116952023	0.00150
NM_153717.3(EVC):c.1528G>A (p.Val510Ile)	rs143971158
NM_153717.3(EVC):c.2449+15del	rs398092136
NM_153717.3(EVC):c.802-17TTC[4]	rs370315662

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