List of variants in gene LDB3 reported as likely benign by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP
NM_007078.3(LDB3):c.1422G>A (p.Ser474=)	rs142625982
NM_007078.3(LDB3):c.1653C>T (p.Cys551=)	rs45581435
NM_007078.3(LDB3):c.1896C>A (p.Thr632=)
NM_007078.3(LDB3):c.2130C>T (p.Tyr710=)
NM_007078.3(LDB3):c.336C>T (p.Asp112=)	rs776688376
NM_007078.3(LDB3):c.465C>T (p.Leu155=)	rs45516997
NM_007078.3(LDB3):c.543C>T (p.Leu181=)	rs148324530
NM_007078.3(LDB3):c.752A>G (p.Lys251Arg)	rs34423165
NM_007078.3(LDB3):c.993G>A (p.Ala331=)	rs140347820

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.