ClinVar Miner

List of variants in gene LDB3 reported as benign for not provided

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Total variants: 46
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HGVS dbSNP
NM_001368063.1(LDB3):c.-23-259G>T
NM_001368063.1(LDB3):c.-23-268T>C
NM_001368063.1(LDB3):c.-23-350A>T
NM_001368063.1(LDB3):c.-23-379G>A
NM_007078.3(LDB3):c.1014A>G (p.Thr338=) rs150209221
NM_007078.3(LDB3):c.1074C>T (p.Ala358=) rs45459491
NM_007078.3(LDB3):c.1086-75G>T
NM_007078.3(LDB3):c.1231+240G>A
NM_007078.3(LDB3):c.1231+30C>G rs11597201
NM_007078.3(LDB3):c.1232-100G>A
NM_007078.3(LDB3):c.1232-278G>A
NM_007078.3(LDB3):c.1232-96A>C
NM_007078.3(LDB3):c.163G>A (p.Val55Ile) rs3740343
NM_007078.3(LDB3):c.1676+250G>A
NM_007078.3(LDB3):c.1677-197G>A
NM_007078.3(LDB3):c.1978+175G>A
NM_007078.3(LDB3):c.1978+284G>T
NM_007078.3(LDB3):c.1979-174T>G
NM_007078.3(LDB3):c.2016C>T (p.Cys672=) rs45578640
NM_007078.3(LDB3):c.2094+94del
NM_007078.3(LDB3):c.2095-235G>C
NM_007078.3(LDB3):c.2095-282G>A
NM_007078.3(LDB3):c.2095-295C>G
NM_007078.3(LDB3):c.245+156A>C
NM_007078.3(LDB3):c.245+278T>C
NM_007078.3(LDB3):c.246-162C>T
NM_007078.3(LDB3):c.321+104G>A
NM_007078.3(LDB3):c.321+192G>C
NM_007078.3(LDB3):c.321+248G>A
NM_007078.3(LDB3):c.322-156T>C
NM_007078.3(LDB3):c.322-161A>G
NM_007078.3(LDB3):c.322-197C>G
NM_007078.3(LDB3):c.322-290C>G
NM_007078.3(LDB3):c.576G>A (p.Pro192=) rs45543741
NM_007078.3(LDB3):c.576G>T (p.Pro192=) rs45543741
NM_007078.3(LDB3):c.689+149A>G
NM_007078.3(LDB3):c.690-228del
NM_007078.3(LDB3):c.859+47G>C rs3740346
NM_007078.3(LDB3):c.896+45G>A
NM_007078.3(LDB3):c.897-304A>C
NM_007078.3(LDB3):c.93+165C>A
NM_007078.3(LDB3):c.93+177C>T
NM_007078.3(LDB3):c.94-119G>A
NM_007078.3(LDB3):c.94-124G>A
NM_007078.3(LDB3):c.94-294T>C
NM_007078.3(LDB3):c.993G>A (p.Ala331=) rs140347820

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