ClinVar Miner

List of variants in gene SBF2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_030962.4(SBF2):c.3979-256C>T rs139479293 0.02070
NM_030962.4(SBF2):c.141+258C>T rs185107978 0.02013
NM_030962.4(SBF2):c.1601-274C>T rs12276925 0.01802
NM_030962.4(SBF2):c.1395+74C>T rs34611271 0.01618
NM_030962.4(SBF2):c.1396-87G>A rs114180283 0.01383
NM_030962.4(SBF2):c.862-254A>T rs117107002 0.01381
NM_030962.4(SBF2):c.280-193G>A rs141773803 0.01339
NM_030962.4(SBF2):c.1860+101A>G rs16907298 0.01313
NM_030962.4(SBF2):c.1167+64G>T rs60333011 0.01221
NM_030962.4(SBF2):c.403-315G>A rs73410824 0.01176
NM_030962.4(SBF2):c.403-82A>G rs73410823 0.01173
NM_030962.4(SBF2):c.3793+235T>A rs74578546 0.00947
NM_030962.4(SBF2):c.1711-327G>A rs56393596 0.00894
NM_030962.4(SBF2):c.1296+32A>G rs73406739 0.00891
NM_030962.4(SBF2):c.*177A>C rs192542785 0.00872
NM_030962.4(SBF2):c.4155+191A>G rs80166633 0.00858
NM_030962.4(SBF2):c.*51T>C rs41275194 0.00749
NM_030962.4(SBF2):c.753-80C>T rs140138632 0.00724
NM_030962.4(SBF2):c.1860+73T>A rs74997924 0.00696
NM_030962.4(SBF2):c.1296+296A>G rs182844619 0.00649
NM_030962.4(SBF2):c.1167+57C>T rs139290061 0.00641
NM_030962.4(SBF2):c.862-99A>C rs145988551 0.00508
NM_030962.4(SBF2):c.-118G>T rs563422015 0.00491
NM_030962.4(SBF2):c.56-219T>C rs76617958 0.00488
NM_030962.4(SBF2):c.3652+201T>A rs112355769 0.00446
NC_000011.10:g.10294293C>G rs553137073 0.00428
NM_030962.4(SBF2):c.280-122A>T rs182780882 0.00394
NM_030962.4(SBF2):c.1296+149C>T rs192948025 0.00391
NC_000011.10:g.10294362G>C rs537734020 0.00388
NM_030962.4(SBF2):c.55+138C>T rs570399998 0.00388
NM_030962.4(SBF2):c.1168-145C>T rs188819573 0.00385
NM_030962.4(SBF2):c.1053+122A>G rs145969395 0.00384
NM_030962.4(SBF2):c.753-333A>G rs574226051 0.00383
NM_030962.4(SBF2):c.3653-203T>A rs185605599 0.00381
NM_030962.4(SBF2):c.975+317C>T rs114839239 0.00368
NM_030962.4(SBF2):c.4444-18T>G rs143439179 0.00041
NM_030962.4(SBF2):c.291G>A (p.Lys97=) rs150056369 0.00039
NM_030962.4(SBF2):c.1509A>G (p.Glu503=) rs143773975 0.00030
NM_030962.4(SBF2):c.3819C>T (p.Ser1273=) rs145351367 0.00030
NM_030962.4(SBF2):c.513+18A>T rs201201683 0.00027
NM_030962.4(SBF2):c.4128G>A (p.Ala1376=) rs191964053 0.00017
NM_030962.4(SBF2):c.514-12C>T rs770141264 0.00016
NM_030962.4(SBF2):c.1812C>T (p.Asp604=) rs765658939 0.00015
NM_030962.4(SBF2):c.4095C>T (p.Ile1365=) rs142904756 0.00011
NM_030962.4(SBF2):c.946C>T (p.Leu316=) rs374841593 0.00008
NM_030962.4(SBF2):c.129G>A (p.Gln43=) rs761285505 0.00004
NM_030962.4(SBF2):c.403-15T>G rs887143579 0.00003
NM_030962.4(SBF2):c.993G>A (p.Leu331=) rs766193938 0.00003
NM_030962.4(SBF2):c.142-11A>G rs539146891 0.00002
NM_030962.4(SBF2):c.402+15G>A rs780717348 0.00002
NM_030962.4(SBF2):c.4068G>A (p.Leu1356=) rs1429589073 0.00001
NM_030962.4(SBF2):c.4509C>T (p.His1503=) rs138816399 0.00001
NM_030962.4(SBF2):c.620-9T>C rs199676895 0.00001
NM_030962.4(SBF2):c.*20C>G rs1057523279
NM_030962.4(SBF2):c.1054-11T>C rs1554976748
NM_030962.4(SBF2):c.1396-295T>C rs77182089
NM_030962.4(SBF2):c.142-14dup rs530695547
NM_030962.4(SBF2):c.1491T>C (p.Asn497=) rs767806871
NM_030962.4(SBF2):c.1601-309C>T rs187222593
NM_030962.4(SBF2):c.1710+181_1710+184dup rs530782404
NM_030962.4(SBF2):c.1860+10A>G rs778305149
NM_030962.4(SBF2):c.3652+6C>T rs1057524041
NM_030962.4(SBF2):c.3652+9CT[2] rs376260584
NM_030962.4(SBF2):c.3653-76GATA[6] rs143416649
NM_030962.4(SBF2):c.3979-4G>T rs375742620
NM_030962.4(SBF2):c.403-335dup rs533328520
NM_030962.4(SBF2):c.492C>G (p.Val164=) rs559769224
NM_030962.4(SBF2):c.513+297G>A rs181190005
NM_030962.4(SBF2):c.753-16T>C rs7128234
NM_030962.4(SBF2):c.807A>T (p.Pro269=) rs1057521879
NM_030962.4(SBF2):c.861+308C>A rs73408778
NM_030962.4(SBF2):c.862-9C>A rs1554979581
NM_030962.4(SBF2):c.976-195C>T rs537420042

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