ClinVar Miner

List of variants in gene NSD2 reported as uncertain significance for Wolf-Hirschhorn syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_133330.2(NSD2):c.*118G>A rs886059320
NM_133330.2(NSD2):c.*1370dupT rs886059325
NM_133330.2(NSD2):c.*1458G>C rs886059326
NM_133330.2(NSD2):c.*1468G>C rs886059327
NM_133330.2(NSD2):c.*1572A>G rs886059328
NM_133330.2(NSD2):c.*1665C>T rs539743018
NM_133330.2(NSD2):c.*1686C>T rs74372602
NM_133330.2(NSD2):c.*1757C>T rs886059329
NM_133330.2(NSD2):c.*1777C>T rs886059330
NM_133330.2(NSD2):c.*1844T>C rs755058552
NM_133330.2(NSD2):c.*1850G>A rs765387218
NM_133330.2(NSD2):c.*1922dupT rs886059331
NM_133330.2(NSD2):c.*1942T>C rs780819245
NM_133330.2(NSD2):c.*2003T>G rs886059332
NM_133330.2(NSD2):c.*2012dupG rs766138833
NM_133330.2(NSD2):c.*2020G>A rs778656433
NM_133330.2(NSD2):c.*2414G>A rs886059334
NM_133330.2(NSD2):c.*2423G>A rs886059335
NM_133330.2(NSD2):c.*2603A>T rs886059336
NM_133330.2(NSD2):c.*2811C>T rs149980218
NM_133330.2(NSD2):c.*2812G>A rs886059337
NM_133330.2(NSD2):c.*2847T>G rs886059338
NM_133330.2(NSD2):c.*3186T>C rs762277303
NM_133330.2(NSD2):c.*661G>A rs767998808
NM_133330.2(NSD2):c.*731G>A rs886059322
NM_133330.2(NSD2):c.*745T>C rs886059323
NM_133330.2(NSD2):c.*986G>A rs886059324
NM_133330.2(NSD2):c.-166C>A rs372789667
NM_133330.2(NSD2):c.-185G>A rs886059312
NM_133330.2(NSD2):c.-218T>G rs544091833
NM_133330.2(NSD2):c.-280T>G rs886059311
NM_133330.2(NSD2):c.-348A>T rs886059310
NM_133330.2(NSD2):c.-384-3C>T rs886059309
NM_133330.2(NSD2):c.-384-5dupT rs886059308
NM_133330.2(NSD2):c.-390T>A rs566943306
NM_133330.2(NSD2):c.-402A>C rs886059307
NM_133330.2(NSD2):c.-434C>G rs886059306
NM_133330.2(NSD2):c.-44C>T rs886059313
NM_133330.2(NSD2):c.-62T>C rs774930051
NM_133330.2(NSD2):c.114C>T (p.Cys38=) rs759922625
NM_133330.2(NSD2):c.11G>A (p.Ser4Asn) rs753120179
NM_133330.2(NSD2):c.1653G>A (p.Thr551=) rs141132577
NM_133330.2(NSD2):c.1675-10T>A rs886059317
NM_133330.2(NSD2):c.1881+9A>T rs767417151
NM_133330.2(NSD2):c.1902C>T (p.Asp634=) rs746926553
NM_133330.2(NSD2):c.199G>A (p.Gly67Ser) rs202235551
NM_133330.2(NSD2):c.2414T>C (p.Val805Ala) rs144335923
NM_133330.2(NSD2):c.2831G>A (p.Arg944Gln) rs756624618
NM_133330.2(NSD2):c.3126C>T (p.His1042=) rs886059318
NM_133330.2(NSD2):c.3486C>T (p.Gly1162=) rs886059319
NM_133330.2(NSD2):c.456T>G (p.Ser152=) rs886059314
NM_133330.2(NSD2):c.546C>A (p.Gly182=) rs766214080
NM_133330.2(NSD2):c.562C>G (p.Leu188Val) rs886059315
NM_133330.2(NSD2):c.576C>T (p.Ile192=) rs138137147
NM_133330.2(NSD2):c.927+15T>C rs886059316
NM_133330.2(NSD2):c.940A>G (p.Ile314Val) rs371529672

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