ClinVar Miner

List of variants in gene EYS reported as benign

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Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP
GRCh37/hg19 6q12(chr6:64658077-64695023)x1
GRCh37/hg19 6q12(chr6:64662711-64668193)x0
GRCh37/hg19 6q12(chr6:64667045-64680963)x0
GRCh37/hg19 6q12(chr6:64667045-64693014)x1
GRCh37/hg19 6q12(chr6:65187445-65227097)x1
GRCh37/hg19 6q12(chr6:65307434-65328120)x1
GRCh37/hg19 6q12(chr6:65347424-65354108)x0
GRCh37/hg19 6q12(chr6:65347533-65365420)x3
GRCh37/hg19 6q12(chr6:65635578-65734358)x1
GRCh37/hg19 6q12(chr6:65711755-65726738)x1
GRCh37/hg19 6q12(chr6:65715716-65836765)x1
GRCh37/hg19 6q12(chr6:65763048-65790983)x1
GRCh37/hg19 6q12(chr6:65786994-65814638)x1
GRCh37/hg19 6q12(chr6:65825391-65918649)x1
GRCh37/hg19 6q12(chr6:65828853-65910600)x1
GRCh37/hg19 6q12(chr6:65903328-65910600)x1
GRCh37/hg19 6q12(chr6:65909976-65910600)x1
GRCh37/hg19 6q12(chr6:66377946-66442496)x3
GRCh37/hg19 6q12(chr6:66391650-66506140)x1
GRCh37/hg19 6q12(chr6:66397288-66405466)x3
GRCh37/hg19 6q12(chr6:66402855-66404622)x3
GRCh37/hg19 6q12(chr6:66402855-66405466)x3
GRCh37/hg19 6q12(chr6:66402855-66414828)x4
GRCh37/hg19 6q12(chr6:66403264-66414828)x3
NM_001142800.1(EYS):c.1146T>C (p.Asn382=) rs974110
NM_001142800.1(EYS):c.1300-3C>T rs1936439
NM_001142800.1(EYS):c.1599+13T>C rs182876572
NM_001142800.1(EYS):c.1712A>G (p.Gln571Arg) rs61753610
NM_001142800.1(EYS):c.1809C>T (p.Val603=) rs9345601
NM_001142800.1(EYS):c.1891G>A (p.Gly631Ser) rs9342464
NM_001142800.1(EYS):c.1922A>T (p.Glu641Val) rs17411795
NM_001142800.1(EYS):c.1985G>T (p.Arg662Met) rs144430026
NM_001142800.1(EYS):c.2023+15dupT rs35045551
NM_001142800.1(EYS):c.2024-14C>T rs45628235
NM_001142800.1(EYS):c.2500G>A (p.Val834Ile) rs112464110
NM_001142800.1(EYS):c.2555T>C (p.Leu852Pro) rs9294631
NM_001142800.1(EYS):c.2733T>C (p.Asn911=) rs75634595
NM_001142800.1(EYS):c.334G>A (p.Val112Ile) rs112609906
NM_001142800.1(EYS):c.359C>T (p.Thr120Met) rs12193967
NM_001142800.1(EYS):c.3787A>G (p.Ile1263Val) rs17404123
NM_001142800.1(EYS):c.3877+18_3877+22delAGATA rs139235690
NM_001142800.1(EYS):c.3906C>T (p.His1302=) rs12663916
NM_001142800.1(EYS):c.3936A>G (p.Thr1312=) rs12662610
NM_001142800.1(EYS):c.3973C>G (p.Gln1325Glu) rs12663622
NM_001142800.1(EYS):c.4026C>T (p.Ser1342=) rs12663619
NM_001142800.1(EYS):c.4081A>G (p.Ile1361Val) rs17403955
NM_001142800.1(EYS):c.4093A>G (p.Lys1365Glu) rs16895519
NM_001142800.1(EYS):c.4256T>C (p.Leu1419Ser) rs624851
NM_001142800.1(EYS):c.4352T>C (p.Ile1451Thr) rs62415828
NM_001142800.1(EYS):c.4543C>T (p.Arg1515Trp) rs62415827
NM_001142800.1(EYS):c.4549A>G (p.Ser1517Gly) rs62415826
NM_001142800.1(EYS):c.4593G>A (p.Glu1531=) rs62415825
NM_001142800.1(EYS):c.5244A>C (p.Leu1748Phe) rs57312007
NM_001142800.1(EYS):c.5601T>C (p.Ser1867=) rs182322608
NM_001142800.1(EYS):c.5617C>G (p.Leu1873Val) rs16895517
NM_001142800.1(EYS):c.5705A>T (p.Asn1902Ile) rs9353806
NM_001142800.1(EYS):c.5977A>G (p.Thr1993Ala) rs115066356
NM_001142800.1(EYS):c.6079-4_6079-3delTC rs35395170
NM_001142800.1(EYS):c.6119T>A (p.Val2040Asp) rs201580493
NM_001142800.1(EYS):c.6977G>A (p.Arg2326Gln) rs4710457
NM_001142800.1(EYS):c.7666A>T (p.Ser2556Cys) rs66462731
NM_001142800.1(EYS):c.8429C>T (p.Thr2810Ile) rs144513453
NM_001142800.1(EYS):c.9030A>G (p.Ala3010=) rs61754905
NM_001142800.1(EYS):c.9345_9347delTGT (p.Val3116del) rs536788112
NM_001142800.1(EYS):c.988G>A (p.Glu330Lys) rs144803840
NM_001292009.1(EYS):c.2259+10C>T rs78511049
NM_001292009.1(EYS):c.5044G>T (p.Asp1682Tyr) rs75831552

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