Variants in gene LDB3 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.690-4A>G	rs45529531	0.00427
NM_007078.3(LDB3):c.466G>A (p.Ala156Thr)	rs200596619	0.00082
NM_007078.3(LDB3):c.1535A>C (p.Gln512Pro)	rs138951890	0.00080
NM_001368067.1(LDB3):c.771G>A (p.Thr257=)	rs144445130	0.00040
NM_007078.3(LDB3):c.1049C>T (p.Thr350Ile)	rs200796750	0.00022
NM_007078.3(LDB3):c.1672A>G (p.Ile558Val)	rs372331627	0.00003
NM_007078.3(LDB3):c.723C>T (p.Ser241=)	rs200580597	0.00001
NM_007078.3(LDB3):c.1325C>T (p.Ala442Val)	rs786205349
NM_007078.3(LDB3):c.897-6707G>A	rs537660741

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