ClinVar Miner

List of variants reported as likely benign for Wolf-Hirschhorn syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_001042424.3(NSD2):c.*1025C>A rs548104599
NM_001042424.3(NSD2):c.*1085A>T rs111668967
NM_001042424.3(NSD2):c.*1138G>C rs77074637
NM_001042424.3(NSD2):c.*1297A>G rs184511643
NM_001042424.3(NSD2):c.*148C>T rs538719785
NM_001042424.3(NSD2):c.*167A>G rs114883490
NM_001042424.3(NSD2):c.*176C>T rs187504628
NM_001042424.3(NSD2):c.*183T>C rs192992535
NM_001042424.3(NSD2):c.*1849C>T rs562324621
NM_001042424.3(NSD2):c.*2094C>T rs141972110
NM_001042424.3(NSD2):c.*2121C>T rs116110889
NM_001042424.3(NSD2):c.*2337A>C rs146115430
NM_001042424.3(NSD2):c.*2355G>A rs140096622
NM_001042424.3(NSD2):c.*2521A>G rs180696589
NM_001042424.3(NSD2):c.*2634C>T rs112691599
NM_001042424.3(NSD2):c.*2733G>C rs73796676
NM_001042424.3(NSD2):c.*2780G>A rs139523257
NM_001042424.3(NSD2):c.*2917C>G rs145672223
NM_001042424.3(NSD2):c.*2920A>G rs2187692
NM_001042424.3(NSD2):c.*2938_*2941TGTT[1] rs147409255
NM_001042424.3(NSD2):c.*296A>G rs114085362
NM_001042424.3(NSD2):c.*3199G>T rs14647
NM_001042424.3(NSD2):c.*3208A>G rs142634124
NM_001042424.3(NSD2):c.*3241A>C rs569244997
NM_001042424.3(NSD2):c.*339_*341CTC[1] rs375129793
NM_001042424.3(NSD2):c.*524G>A rs112146288
NM_001042424.3(NSD2):c.*593G>T rs73202837
NM_001042424.3(NSD2):c.*620T>A rs1132849
NM_001042424.3(NSD2):c.*620T>G rs1132849
NM_001042424.3(NSD2):c.*674A>G rs115893772
NM_001042424.3(NSD2):c.*870A>C rs117600071
NM_001042424.3(NSD2):c.*969G>A rs562124371
NM_001042424.3(NSD2):c.*9G>A rs373762613
NM_001042424.3(NSD2):c.-29-1244G>A rs116056077
NM_001042424.3(NSD2):c.-29-1260A>G rs147609440
NM_001042424.3(NSD2):c.-29-1320G>A rs550551908
NM_001042424.3(NSD2):c.-29-1346C>T rs569542496
NM_001042424.3(NSD2):c.-29-6719G>A rs114792920
NM_001042424.3(NSD2):c.-29-7808C>T rs184985997
NM_001042424.3(NSD2):c.1330A>G (p.Thr444Ala) rs112014939
NM_001042424.3(NSD2):c.1582C>A (p.His528Asn) rs139753036
NM_001042424.3(NSD2):c.1584C>A (p.His528Gln) rs149810908
NM_001042424.3(NSD2):c.198C>T (p.Asn66=) rs140040537
NM_001042424.3(NSD2):c.216C>G (p.Pro72=) rs112939388
NM_001042424.3(NSD2):c.228C>T (p.Ala76=) rs74665455
NM_001042424.3(NSD2):c.2352G>T (p.Arg784=) rs531537433
NM_001042424.3(NSD2):c.2814G>A (p.Pro938=) rs62287053
NM_001042424.3(NSD2):c.3474C>T (p.Asp1158=) rs138946638
NM_001042424.3(NSD2):c.3495C>T (p.Ala1165=) rs73069117
NM_001042424.3(NSD2):c.3582A>G (p.Gly1194=) rs149284685
NM_001042424.3(NSD2):c.381A>G (p.Lys127=) rs149396950
NM_001042424.3(NSD2):c.3900C>T (p.Pro1300=) rs75949599
NM_001042424.3(NSD2):c.4023C>T (p.Pro1341=) rs149925711
NM_001042424.3(NSD2):c.4026C>G (p.Pro1342=) rs147624398
NM_001042424.3(NSD2):c.884A>T (p.Gln295Leu) rs144431814
NM_001042424.3(NSD2):c.990A>G (p.Glu330=) rs143425918

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