ClinVar Miner

List of variants reported as benign for Dilated cardiomyopathy 1J

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_004100.5(EYA4):c.*1264T>A rs9483585 0.99999
NM_004100.5(EYA4):c.*1434A>G rs9483586 0.79868
NM_004100.5(EYA4):c.1281+21A>G rs2277083 0.62034
NM_004100.5(EYA4):c.829G>A (p.Gly277Ser) rs9493627 0.37885
NM_004100.5(EYA4):c.*23C>T rs3734279 0.35809
NM_004100.5(EYA4):c.*2108A>G rs17053541 0.24433
NM_004100.5(EYA4):c.*2184A>T rs17053542 0.20492
NM_004100.5(EYA4):c.*726C>A rs55805978 0.20466
NM_004100.5(EYA4):c.*1867C>T rs17053540 0.15248
NM_004100.5(EYA4):c.*1658C>T rs73546865 0.04226
NM_004100.5(EYA4):c.-76C>T rs78081370 0.04026
NM_004100.5(EYA4):c.804+17T>C rs57845656 0.01673
NM_004100.5(EYA4):c.905G>A (p.Gly302Asp) rs75133151 0.00860
NM_004100.5(EYA4):c.1845C>T (p.Asn615=) rs142721902 0.00854
NM_004100.5(EYA4):c.111T>C (p.Ser37=) rs35863035 0.00620
NM_004100.5(EYA4):c.103C>T (p.Leu35=) rs35562371 0.00597
NM_004100.5(EYA4):c.804+16G>T rs13362743 0.00276
NM_004100.5(EYA4):c.783G>A (p.Thr261=) rs17854076 0.00136
NM_004100.5(EYA4):c.277+9G>A rs145320803 0.00072
NM_004100.5(EYA4):c.1281+20C>T rs76551188 0.00069
NM_004100.5(EYA4):c.1329G>A (p.Gly443=) rs141300030 0.00067
NM_004100.5(EYA4):c.970+16C>G rs201985955 0.00033
NM_004100.5(EYA4):c.1617-13C>G rs756045097 0.00018
NM_004100.5(EYA4):c.1501+19A>G rs200678450 0.00015
NM_004100.5(EYA4):c.1418G>T (p.Gly473Val) rs146977269 0.00014
NM_004100.5(EYA4):c.873A>T (p.Gly291=) rs761206775 0.00003
NM_004100.5(EYA4):c.580+14_580+16del rs139659489
NM_004100.5(EYA4):c.725-9del rs776867589
NM_004100.5(EYA4):c.867G>A (p.Thr289=) rs763899252
NM_004100.5(EYA4):c.925A>G (p.Thr309Ala) rs556335059

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