List of variants in gene EVC reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_153717.3(EVC):c.1826G>A (p.Arg609Gln)	rs41269557	0.00201
NM_153717.3(EVC):c.550G>A (p.Asp184Asn)	rs41269549	0.00194
NM_153717.3(EVC):c.934G>A (p.Asp312Asn)	rs115275195	0.00171
NM_153717.3(EVC):c.89C>T (p.Pro30Leu)	rs886044558	0.00121
NM_153717.3(EVC):c.2350G>A (p.Ala784Thr)	rs149537641	0.00024
NM_153717.3(EVC):c.1777G>A (p.Val593Met)	rs150535483	0.00014
NM_153717.3(EVC):c.940-150T>C	rs576076928	0.00006
NM_153717.3(EVC):c.2305-6C>T	rs781705295	0.00004
NM_153717.3(EVC):c.625G>A (p.Val209Ile)	rs202026284	0.00003
NM_153717.3(EVC):c.1955G>A (p.Arg652His)	rs765024763	0.00001
NM_153717.3(EVC):c.2740C>T (p.Leu914Phe)	rs370825749	0.00001
NM_153717.3(EVC):c.928C>G (p.Leu310Val)	rs145300726	0.00001
NM_153717.3(EVC):c.1652C>G (p.Pro551Arg)	rs371682994
NM_153717.3(EVC):c.2152C>T (p.Arg718Trp)

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