List of variants in gene LDB3 reported as benign by Ambry Genetics

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: 15

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HGVS	dbSNP	gnomAD frequency
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.752A>G (p.Lys251Arg)	rs34423165	0.01671
NM_007078.3(LDB3):c.609G>A (p.Ser203=)	rs45531131	0.01554
NM_007078.3(LDB3):c.302C>T (p.Pro101Leu)	rs45592139	0.00960
NM_007078.3(LDB3):c.1506G>A (p.Pro502=)	rs45579241	0.00941
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.1263G>A (p.Gly421=)	rs139834701	0.00369
NM_007078.3(LDB3):c.163G>A (p.Val55Ile)	rs3740343	0.00292
NM_007078.3(LDB3):c.295C>T (p.Pro99Ser)	rs201693259	0.00088
NM_007078.3(LDB3):c.1335C>T (p.Tyr445=)	rs587781024	0.00017
NM_007078.3(LDB3):c.273G>A (p.Thr91=)	rs45613039	0.00010
NM_007078.3(LDB3):c.1041C>A (p.Ser347=)	rs45555240
NM_007078.3(LDB3):c.576G>T (p.Pro192=)	rs45543741

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