ClinVar Miner

List of variants in gene EYA1 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP
NM_000503.5(EYA1):c.*1914T>G rs112480709
NM_000503.6(EYA1):c.*1217_*1219TTA[1] rs574723016
NM_000503.6(EYA1):c.*1222A>C rs117394899
NM_000503.6(EYA1):c.*1263C>T rs140308724
NM_000503.6(EYA1):c.*1275G>A rs192113669
NM_000503.6(EYA1):c.*1310G>A rs147323889
NM_000503.6(EYA1):c.*1561_*1564ATCA[3] rs553875263
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.*705G>T rs79700717
NM_000503.6(EYA1):c.*784T>C rs77243350
NM_000503.6(EYA1):c.*86C>A rs186838732
NM_000503.6(EYA1):c.-191C>G rs55694100
NM_000503.6(EYA1):c.-340G>T rs55997623
NM_000503.6(EYA1):c.-454G>A rs569684779
NM_000503.6(EYA1):c.-49A>G rs773963094
NM_000503.6(EYA1):c.1141-15T>G rs186249248
NM_000503.6(EYA1):c.1200-11C>A rs181457812
NM_000503.6(EYA1):c.1258T>C (p.Leu420=) rs200074362
NM_000503.6(EYA1):c.1276G>A (p.Gly426Ser) rs121909199
NM_000503.6(EYA1):c.1460C>T (p.Ser487Leu) rs139717960
NM_000503.6(EYA1):c.1475+15G>A rs373917012
NM_000503.6(EYA1):c.164C>T (p.Thr55Met) rs201434219
NM_000503.6(EYA1):c.1699-3C>T rs117149407
NM_000503.6(EYA1):c.1699-8T>C rs201537030
NM_000503.6(EYA1):c.648G>A (p.Pro216=) rs148973681
NM_000503.6(EYA1):c.743C>T (p.Thr248Met) rs186736708
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.840C>A (p.Ile280=) rs55972891
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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