List of variants in gene LDB3 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.1074C>T (p.Ala358=)	rs45459491	0.02688
NM_007078.3(LDB3):c.1903G>A (p.Val635Ile)	rs45618633	0.01846
NM_007078.3(LDB3):c.752A>G (p.Lys251Arg)	rs34423165	0.01671
NM_007078.3(LDB3):c.302C>T (p.Pro101Leu)	rs45592139	0.00960
NM_007078.3(LDB3):c.1014A>G (p.Thr338=)	rs150209221	0.00450
NM_007078.3(LDB3):c.147G>A (p.Val49=)	rs45591834	0.00312
NM_007078.3(LDB3):c.2016C>T (p.Cys672=)	rs45578640	0.00288
NM_007078.3(LDB3):c.1460G>A (p.Arg487His)	rs146265188	0.00189
NM_007078.3(LDB3):c.954C>T (p.Pro318=)	rs45603139	0.00168
NM_007078.3(LDB3):c.1422G>A (p.Ser474=)	rs142625982	0.00136
NM_007078.3(LDB3):c.689+10G>A	rs45563234	0.00125
NM_007078.3(LDB3):c.1653C>T (p.Cys551=)	rs45581435	0.00096
NM_007078.3(LDB3):c.993G>A (p.Ala331=)	rs140347820	0.00095
NM_007078.3(LDB3):c.1035C>T (p.Ile345=)	rs121908336	0.00029
NM_007078.3(LDB3):c.1971C>T (p.Cys657=)	rs140552419	0.00025
NM_007078.3(LDB3):c.897-14T>C	rs763081924	0.00014
NM_007078.3(LDB3):c.1956C>T (p.Asp652=)	rs139213290	0.00013
NM_007078.3(LDB3):c.714C>T (p.Ala238=)	rs727503125	0.00013
NM_007078.3(LDB3):c.897-16G>C	rs45513100	0.00011
NM_007078.3(LDB3):c.273G>A (p.Thr91=)	rs45613039	0.00010
NM_007078.3(LDB3):c.891G>A (p.Arg297=)	rs374336814	0.00010
NM_007078.3(LDB3):c.1521C>T (p.Thr507=)	rs200838004	0.00006
NM_007078.3(LDB3):c.689+9C>T	rs727503124	0.00006
NM_007078.3(LDB3):c.900C>A (p.Thr300=)	rs760071118	0.00003
NM_007078.3(LDB3):c.2091C>T (p.Cys697=)	rs571356142	0.00001
NM_007078.3(LDB3):c.1041C>A (p.Ser347=)	rs45555240
NM_007078.3(LDB3):c.1232-12dup	rs752301693
NM_007078.3(LDB3):c.1296_1343del (p.Ala434_Pro449del)	rs397517209
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.576G>T (p.Pro192=)	rs45543741

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