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: 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.752A>G (p.Lys251Arg)	rs34423165	0.01591
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.1594G>C (p.Ala532Pro)	rs143764931	0.00036
NM_007078.3(LDB3):c.664G>A (p.Ala222Thr)	rs139922045	0.00036
NM_007078.3(LDB3):c.1051A>G (p.Thr351Ala)	rs138251566	0.00026
NM_007078.3(LDB3):c.1071T>A (p.Pro357=)	rs143823978	0.00008
NM_007078.3(LDB3):c.543C>T (p.Leu181=)	rs148324530	0.00005
NM_007078.3(LDB3):c.336C>T (p.Asp112=)	rs776688376	0.00001
NM_007078.3(LDB3):c.540A>G (p.Leu180=)	rs1283051092	0.00001
NM_007078.3(LDB3):c.1896C>A (p.Thr632=)	rs1846967797
NM_007078.3(LDB3):c.2130C>T (p.Tyr710=)	rs752415111
NM_007078.3(LDB3):c.465C>T (p.Leu155=)	rs45516997

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