ClinVar Miner

List of variants in gene LDB3 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP
NM_001080116.1(LDB3):c.771G>A (p.Thr257=) rs144445130
NM_001368063.1(LDB3):c.-23-259G>T rs11812601
NM_001368063.1(LDB3):c.-23-268T>C rs2803555
NM_001368063.1(LDB3):c.-23-350A>T rs2675692
NM_001368063.1(LDB3):c.-23-379G>A rs35777670
NM_007078.3(LDB3):c.-24+8T>C rs2803558
NM_007078.3(LDB3):c.-36A>G rs2803557
NM_007078.3(LDB3):c.-48G>A rs2803556
NM_007078.3(LDB3):c.-49C>T rs146911972
NM_007078.3(LDB3):c.1035C>T (p.Ile345=) rs121908336
NM_007078.3(LDB3):c.1086-75G>T rs3740347
NM_007078.3(LDB3):c.1231+19G>A rs763969244
NM_007078.3(LDB3):c.1231+240G>A rs10887651
NM_007078.3(LDB3):c.1231+30C>G rs11597201
NM_007078.3(LDB3):c.1232-100G>A rs114915313
NM_007078.3(LDB3):c.1232-278G>A rs12218053
NM_007078.3(LDB3):c.1232-96A>C rs59439194
NM_007078.3(LDB3):c.1335C>T (p.Tyr445=) rs587781024
NM_007078.3(LDB3):c.1386C>T (p.Thr462=) rs764330273
NM_007078.3(LDB3):c.1460G>A (p.Arg487His) rs146265188
NM_007078.3(LDB3):c.147G>A (p.Val49=) rs45591834
NM_007078.3(LDB3):c.162C>T (p.Gly54=) rs757856121
NM_007078.3(LDB3):c.1676+250G>A rs7910307
NM_007078.3(LDB3):c.1677-197G>A rs7090715
NM_007078.3(LDB3):c.1903G>A (p.Val635Ile) rs45618633
NM_007078.3(LDB3):c.1956C>T (p.Asp652=) rs139213290
NM_007078.3(LDB3):c.1978+175G>A rs11202138
NM_007078.3(LDB3):c.1978+284G>T rs12219069
NM_007078.3(LDB3):c.1979-174T>G rs7092188
NM_007078.3(LDB3):c.2094+94del rs34647099
NM_007078.3(LDB3):c.2095-235G>C rs7899337
NM_007078.3(LDB3):c.2095-282G>A rs7899324
NM_007078.3(LDB3):c.2095-295C>G rs59412880
NM_007078.3(LDB3):c.245+156A>C rs3740344
NM_007078.3(LDB3):c.245+278T>C rs60835566
NM_007078.3(LDB3):c.246-162C>T rs75738068
NM_007078.3(LDB3):c.321+104G>A rs45598635
NM_007078.3(LDB3):c.321+192G>C rs45519132
NM_007078.3(LDB3):c.321+248G>A rs45617137
NM_007078.3(LDB3):c.322-156T>C rs117975031
NM_007078.3(LDB3):c.322-161A>G rs2675686
NM_007078.3(LDB3):c.322-197C>G rs2248643
NM_007078.3(LDB3):c.322-290C>G rs11813013
NM_007078.3(LDB3):c.352G>A (p.Val118Met) rs35507268
NM_007078.3(LDB3):c.465C>T (p.Leu155=) rs45516997
NM_007078.3(LDB3):c.576G>A (p.Pro192=) rs45543741
NM_007078.3(LDB3):c.689+149A>G rs56165849
NM_007078.3(LDB3):c.690-228del rs11312118
NM_007078.3(LDB3):c.752A>G (p.Lys251Arg) rs34423165
NM_007078.3(LDB3):c.859+14C>G rs748281629
NM_007078.3(LDB3):c.859+47G>C rs3740346
NM_007078.3(LDB3):c.891G>A (p.Arg297=) rs374336814
NM_007078.3(LDB3):c.896+45G>A rs11202128
NM_007078.3(LDB3):c.896+6731C>T rs372789789
NM_007078.3(LDB3):c.896+6823C>T rs377726575
NM_007078.3(LDB3):c.897-304A>C rs17106956
NM_007078.3(LDB3):c.93+165C>A rs12259201
NM_007078.3(LDB3):c.93+177C>T rs3740342
NM_007078.3(LDB3):c.94-119G>A rs4468255
NM_007078.3(LDB3):c.94-124G>A rs12254069
NM_007078.3(LDB3):c.94-294T>C rs112790021

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