ClinVar Miner

List of variants in gene EYA1 reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_000503.6(EYA1):c.*102T>G
NM_000503.6(EYA1):c.*104C>T
NM_000503.6(EYA1):c.*1222A>C rs117394899
NM_000503.6(EYA1):c.*1263C>T rs140308724
NM_000503.6(EYA1):c.*1310G>A rs147323889
NM_000503.6(EYA1):c.*1324T>C rs56115941
NM_000503.6(EYA1):c.*1581G>A rs9298163
NM_000503.6(EYA1):c.*1890A>G rs377092983
NM_000503.6(EYA1):c.*23G>A rs373876510
NM_000503.6(EYA1):c.*353C>T rs151172668
NM_000503.6(EYA1):c.*509_*512del rs146202037
NM_000503.6(EYA1):c.*556A>G
NM_000503.6(EYA1):c.*705G>T rs79700717
NM_000503.6(EYA1):c.*784T>C rs77243350
NM_000503.6(EYA1):c.*800T>C rs74862574
NM_000503.6(EYA1):c.-191C>G rs55694100
NM_000503.6(EYA1):c.-271G>A rs73684755
NM_000503.6(EYA1):c.-340G>T rs55997623
NM_000503.6(EYA1):c.1141-15T>G rs186249248
NM_000503.6(EYA1):c.1185C>T (p.Asn395=) rs372488542
NM_000503.6(EYA1):c.1199+13G>T rs200345478
NM_000503.6(EYA1):c.1200-11C>A rs181457812
NM_000503.6(EYA1):c.121G>C (p.Glu41Gln) rs561111097
NM_000503.6(EYA1):c.1276G>A (p.Gly426Ser) rs121909199
NM_000503.6(EYA1):c.1278C>T (p.Gly426=) rs4738118
NM_000503.6(EYA1):c.1475+15G>A rs373917012
NM_000503.6(EYA1):c.1598-15A>G rs372286227
NM_000503.6(EYA1):c.1699-3C>T rs117149407
NM_000503.6(EYA1):c.1699-8T>C rs201537030
NM_000503.6(EYA1):c.1701C>T (p.His567=) rs763080811
NM_000503.6(EYA1):c.1755T>C (p.His585=) rs10103397
NM_000503.6(EYA1):c.321T>C (p.Ala107=) rs112282055
NM_000503.6(EYA1):c.58C>G (p.Pro20Ala) rs1445404
NM_000503.6(EYA1):c.648G>A (p.Pro216=) rs148973681
NM_000503.6(EYA1):c.724A>G (p.Ser242Gly)
NM_000503.6(EYA1):c.744G>A (p.Thr248=) rs10098224
NM_000503.6(EYA1):c.782C>T (p.Pro261Leu) rs77825059
NM_000503.6(EYA1):c.783G>A (p.Pro261=) rs146648560
NM_000503.6(EYA1):c.813A>G (p.Thr271=) rs1445398
NM_000503.6(EYA1):c.840C>A (p.Ile280=) rs55972891
NM_000503.6(EYA1):c.865G>T (p.Asp289Tyr) rs201504674
NM_000503.6(EYA1):c.887G>A (p.Arg296His)
NM_000503.6(EYA1):c.890G>A (p.Arg297Gln) rs148647933
NM_000503.6(EYA1):c.923G>A (p.Arg308Gln) rs369822742
NM_000503.6(EYA1):c.966+4C>T rs139429307

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