List of variants in gene EYS reported as likely benign for not specified

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001142800.2(EYS):c.6977G>A (p.Arg2326Gln)	rs4710457	0.35152
NM_001142800.2(EYS):c.5705A>T (p.Asn1902Ile)	rs9353806	0.27343
NM_001142800.2(EYS):c.1712A>G (p.Gln571Arg)	rs61753610	0.12981
NM_001142800.2(EYS):c.4352T>C (p.Ile1451Thr)	rs62415828	0.09865
NM_001142800.2(EYS):c.977G>A (p.Ser326Asn)	rs112822256	0.00379
NM_001142800.2(EYS):c.5510G>C (p.Trp1837Ser)	rs199689193	0.00333
NM_001142800.2(EYS):c.4985A>T (p.Asp1662Val)	rs147641443	0.00192
NM_001142800.2(EYS):c.6119T>A (p.Val2040Asp)	rs201580493	0.00166
NM_001142800.2(EYS):c.1184+14T>C	rs182780299	0.00132
NM_001142800.2(EYS):c.2992+12T>A	rs1064794365	0.00001
NM_001142800.2(EYS):c.6025A>G (p.Lys2009Glu)	rs559078881	0.00001
NM_001142800.2(EYS):c.2024-15dup	rs202085379

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