ClinVar Miner

List of variants in gene NF2 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP
NM_000268.3(NF2):c.*1007C>A rs886057350
NM_000268.3(NF2):c.*106C>T rs886057338
NM_000268.3(NF2):c.*109G>T rs886057339
NM_000268.3(NF2):c.*1111G>T rs886057351
NM_000268.3(NF2):c.*1260dup rs886057352
NM_000268.3(NF2):c.*1264C>T rs879093980
NM_000268.3(NF2):c.*1264del rs886057353
NM_000268.3(NF2):c.*1287dup rs886057354
NM_000268.3(NF2):c.*1294T>G rs886057355
NM_000268.3(NF2):c.*1297A>G rs886057356
NM_000268.3(NF2):c.*1326T>C rs886057358
NM_000268.3(NF2):c.*136G>A rs886057340
NM_000268.3(NF2):c.*1439T>C rs886057359
NM_000268.3(NF2):c.*1522C>A rs886057360
NM_000268.3(NF2):c.*1559C>A rs886057361
NM_000268.3(NF2):c.*158T>C rs886057341
NM_000268.3(NF2):c.*1652G>T rs751068883
NM_000268.3(NF2):c.*1672C>T rs757272448
NM_000268.3(NF2):c.*1737C>A rs886057362
NM_000268.3(NF2):c.*1782T>C rs886057363
NM_000268.3(NF2):c.*1848C>T rs886057364
NM_000268.3(NF2):c.*199C>A rs886057342
NM_000268.3(NF2):c.*2003T>G rs886057367
NM_000268.3(NF2):c.*2007del rs886057365
NM_000268.3(NF2):c.*2007dup rs886057365
NM_000268.3(NF2):c.*2010G>T rs886057368
NM_000268.3(NF2):c.*2020C>T rs886057370
NM_000268.3(NF2):c.*2021dup rs886057369
NM_000268.3(NF2):c.*2031_*2032dup rs11442202
NM_000268.3(NF2):c.*2039dup rs886057371
NM_000268.3(NF2):c.*2068G>T rs886057372
NM_000268.3(NF2):c.*2205G>A rs886057373
NM_000268.3(NF2):c.*2206G>A rs886057374
NM_000268.3(NF2):c.*2310C>T rs777037756
NM_000268.3(NF2):c.*2365C>T rs765602116
NM_000268.3(NF2):c.*2373C>A rs886057375
NM_000268.3(NF2):c.*2396G>T rs886057376
NM_000268.3(NF2):c.*2499C>A rs569992376
NM_000268.3(NF2):c.*266G>T rs886057343
NM_000268.3(NF2):c.*2670C>A rs763727745
NM_000268.3(NF2):c.*2753A>G rs199805259
NM_000268.3(NF2):c.*2803C>A rs886057377
NM_000268.3(NF2):c.*293C>A rs886057344
NM_000268.3(NF2):c.*2999G>C rs886057378
NM_000268.3(NF2):c.*3018C>T rs886057379
NM_000268.3(NF2):c.*3055C>T rs886057380
NM_000268.3(NF2):c.*3107T>G rs886057381
NM_000268.3(NF2):c.*3140G>T rs886057382
NM_000268.3(NF2):c.*3189G>T rs886057383
NM_000268.3(NF2):c.*3266C>A rs886057384
NM_000268.3(NF2):c.*3298G>T rs886057385
NM_000268.3(NF2):c.*3319del rs372162228
NM_000268.3(NF2):c.*335C>T rs886057345
NM_000268.3(NF2):c.*3443G>T rs886057387
NM_000268.3(NF2):c.*3480T>G rs886057388
NM_000268.3(NF2):c.*3613_*3618del rs755969033
NM_000268.3(NF2):c.*3646C>T rs886057390
NM_000268.3(NF2):c.*3670C>T rs886057391
NM_000268.3(NF2):c.*3715C>A rs886057392
NM_000268.3(NF2):c.*3783T>C rs886057393
NM_000268.3(NF2):c.*388C>T rs777219109
NM_000268.3(NF2):c.*532G>T rs886057346
NM_000268.3(NF2):c.*561C>G rs776610927
NM_000268.3(NF2):c.*573C>T rs543669369
NM_000268.3(NF2):c.*587G>T rs886057347
NM_000268.3(NF2):c.*768_*769dup rs886057348
NM_000268.3(NF2):c.*987C>A rs886057349
NM_000268.3(NF2):c.-245C>G rs536438675
NM_000268.3(NF2):c.-268G>T rs886057335
NM_000268.3(NF2):c.-284C>A rs886057334
NM_000268.3(NF2):c.-320C>T rs886057333
NM_000268.3(NF2):c.-397C>T rs886057332
NM_000268.3(NF2):c.-402A>G rs886057331
NM_000268.3(NF2):c.1270C>G (p.Arg424Gly) rs763826793
NM_000268.3(NF2):c.1529A>G (p.Lys510Arg) rs886057337
NM_000268.3(NF2):c.676A>C (p.Asn226His) rs886057336

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