List of variants in gene LDB3 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
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.1263G>A (p.Gly421=)	rs139834701	0.00369
NM_007078.3(LDB3):c.-23-32C>A	rs34972863	0.00282
NM_007078.3(LDB3):c.466G>A (p.Ala156Thr)	rs200596619	0.00082
NM_001368067.1(LDB3):c.771G>A (p.Thr257=)	rs144445130	0.00040
NM_007078.3(LDB3):c.897-6707G>A	rs537660741

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