List of variants in gene LDB3 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.352G>A (p.Val118Met)	rs35507268	0.00408
NM_007078.3(LDB3):c.1460G>A (p.Arg487His)	rs146265188	0.00189
NM_007078.3(LDB3):c.1422G>A (p.Ser474=)	rs142625982	0.00136
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.1535A>C (p.Gln512Pro)	rs138951890	0.00080
NM_001368067.1(LDB3):c.780C>T (p.Asn260=)	rs372789789	0.00061
NM_007078.3(LDB3):c.1036G>A (p.Ala346Thr)	rs201968775	0.00054
NM_007078.3(LDB3):c.1111G>A (p.Ala371Thr)	rs45539535	0.00054
NM_007078.3(LDB3):c.1045T>A (p.Ser349Thr)	rs147042608	0.00051
NM_007078.3(LDB3):c.1594G>C (p.Ala532Pro)	rs143764931	0.00036
NM_007078.3(LDB3):c.732C>T (p.Pro244=)	rs144509718	0.00034
NM_007078.3(LDB3):c.1035C>T (p.Ile345=)	rs121908336	0.00029
NM_007078.3(LDB3):c.1051A>G (p.Thr351Ala)	rs138251566	0.00026
NM_007078.3(LDB3):c.1971C>T (p.Cys657=)	rs140552419	0.00025
NM_007078.3(LDB3):c.1503C>T (p.Ala501=)	rs147692024	0.00024
NM_007078.3(LDB3):c.1335C>T (p.Tyr445=)	rs587781024	0.00017
NM_007078.3(LDB3):c.1572G>A (p.Ala524=)	rs149423035	0.00017
NM_007078.3(LDB3):c.159C>T (p.Asp53=)	rs200114285	0.00016
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.1071T>A (p.Pro357=)	rs143823978	0.00009
NM_007078.3(LDB3):c.493C>T (p.Arg165Trp)	rs45610637	0.00009
NM_007078.3(LDB3):c.689+9C>T	rs727503124	0.00006
NM_007078.3(LDB3):c.668C>T (p.Ser223Leu)	rs375306400	0.00005
NM_007078.3(LDB3):c.689+15T>C	rs375094467	0.00004
NM_007078.3(LDB3):c.867C>T (p.Asp289=)	rs397517227	0.00004
NM_007078.3(LDB3):c.1672A>G (p.Ile558Val)	rs372331627	0.00003
NM_007078.3(LDB3):c.1017T>G (p.Ala339=)	rs727504526	0.00001
NM_007078.3(LDB3):c.1605C>T (p.Thr535=)	rs727505207	0.00001
NM_007078.3(LDB3):c.2025C>T (p.Pro675=)	rs876657490	0.00001
NM_007078.3(LDB3):c.2091C>T (p.Cys697=)	rs571356142	0.00001
NM_007078.3(LDB3):c.991G>A (p.Ala331Thr)	rs749520121	0.00001
NM_007078.3(LDB3):c.1041C>T (p.Ser347=)	rs45555240
NM_007078.3(LDB3):c.1167C>T (p.Ala389=)	rs768844187
NM_007078.3(LDB3):c.1317C>T (p.Pro439=)	rs397517208
NM_007078.3(LDB3):c.144C>T (p.Leu48=)	rs397517213
NM_007078.3(LDB3):c.600C>T (p.Gly200=)	rs397517225
NM_007078.3(LDB3):c.896+6669TC[11]	rs71019410
NM_007078.3(LDB3):c.896+6669TC[12]	rs71019410
NM_007078.3(LDB3):c.93+7G>T	rs397517229

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