Variants in gene EYS with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001142800.2(EYS):c.2234A>G (p.Asn745Ser)	rs201652272	0.00066
NM_001142800.2(EYS):c.2137+1G>A	rs199740930	0.00034
NM_001142800.2(EYS):c.6416G>A (p.Cys2139Tyr)	rs749909863	0.00007
NM_001142800.2(EYS):c.35T>C (p.Met12Thr)	rs755947942	0.00006
NM_001142800.2(EYS):c.1765A>G (p.Arg589Gly)	rs778030177	0.00005
NM_001142800.2(EYS):c.6571+5G>A	rs991580368	0.00005
NM_001142800.2(EYS):c.7492G>C (p.Ala2498Pro)	rs1311193836	0.00004
NM_001142800.2(EYS):c.2528G>A (p.Gly843Glu)	rs74419361	0.00002
NM_001142800.2(EYS):c.5644+5G>A	rs794727412	0.00001
NM_001142800.2(EYS):c.1299+5_1299+8del	rs1562140604
NM_001142800.2(EYS):c.732T>A (p.Cys244Ter)	rs1562220891

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