List of variants in gene EVC reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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.89C>T (p.Pro30Leu)	rs886044558	0.00121
NM_153717.3(EVC):c.175-9G>A	rs753317536	0.00001
NM_153717.3(EVC):c.2114A>G (p.Glu705Gly)	rs765248751	0.00001
NM_153717.3(EVC):c.1390C>G (p.Leu464Val)
NM_153717.3(EVC):c.1595A>G (p.Gln532Arg)
NM_153717.3(EVC):c.2580G>C (p.Lys860Asn)

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