ClinVar Miner

List of variants in gene GLB1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000404.4(GLB1):c.793-246A>G rs72856114 0.01967
NC_000003.12:g.33097411C>T rs148730537 0.01878
NM_000404.4(GLB1):c.76-288A>G rs79293183 0.01613
NM_000404.4(GLB1):c.396+61G>A rs78669828 0.01594
NM_000404.4(GLB1):c.246-140G>A rs75415662 0.01577
NM_000404.4(GLB1):c.1480-295A>G rs9860199 0.01493
NM_000404.4(GLB1):c.955+300G>A rs140241744 0.01471
NM_000404.4(GLB1):c.734-116del rs151205825 0.01460
NM_000404.4(GLB1):c.1734+169G>A rs12633200 0.01387
NM_000404.4(GLB1):c.955+206A>G rs145197254 0.01072
NC_000003.12:g.33097543G>A rs142639978 0.00923
NM_000404.4(GLB1):c.1143+47G>A rs139907977 0.00879
NM_000404.4(GLB1):c.552+21G>A rs76275661 0.00847
NM_000404.4(GLB1):c.792+187C>G rs7610177 0.00829
NM_000404.4(GLB1):c.1234-307G>A rs149595582 0.00649
NM_000404.4(GLB1):c.756C>T (p.Phe252=) rs142326197 0.00547
NM_000404.4(GLB1):c.793-69T>C rs150255701 0.00542
NM_000404.4(GLB1):c.1068+291A>C rs570629285 0.00459
NM_000404.4(GLB1):c.245+44A>C rs190936792 0.00275
NM_000404.4(GLB1):c.1233+36A>G rs192752523 0.00272
NM_000404.4(GLB1):c.858C>T (p.Thr286=) rs770638519 0.00002
NM_000404.4(GLB1):c.1143+28G>C rs149712618
NM_000404.4(GLB1):c.245+141A>T rs113835096
NM_000404.4(GLB1):c.457+53C>A rs116227659
NM_000404.4(GLB1):c.955+142_955+143insTTTTCT rs764769471

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