List of variants in gene EVC reported as uncertain significance by Genome-Nilou Lab

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.550G>A (p.Asp184Asn)	rs41269549	0.00194
NM_153717.3(EVC):c.569G>T (p.Arg190Leu)	rs113002470	0.00051
NM_153717.3(EVC):c.2554C>G (p.His852Asp)	rs574669392	0.00002
NM_153717.3(EVC):c.1683C>T (p.Val561=)	rs913909906	0.00001
NM_153717.3(EVC):c.1696G>A (p.Ala566Thr)	rs144943762
NM_153717.3(EVC):c.1988G>C (p.Arg663Pro)	rs372089496

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