List of variants in gene LDB3 reported as benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.859+47G>C	rs3740346	0.13647
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.302C>T (p.Pro101Leu)	rs45592139	0.00960
NM_007078.3(LDB3):c.1014A>G (p.Thr338=)	rs150209221	0.00450
NM_007078.3(LDB3):c.690-4A>G	rs45529531	0.00427
NM_007078.3(LDB3):c.352G>A (p.Val118Met)	rs35507268	0.00408
NM_007078.3(LDB3):c.1263G>A (p.Gly421=)	rs139834701	0.00369
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.954C>T (p.Pro318=)	rs45603139	0.00168
NM_007078.3(LDB3):c.1035C>T (p.Ile345=)	rs121908336	0.00029
NM_007078.3(LDB3):c.1041C>A (p.Ser347=)	rs45555240
NM_007078.3(LDB3):c.1296_1343del (p.Ala434_Pro449del)	rs397517209
NM_007078.3(LDB3):c.1404C>T (p.Asn468=)	rs886038405
NM_007078.3(LDB3):c.690-50G>C	rs886038580

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