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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 3

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HGVS	dbSNP
NM_007078.3(LDB3):c.1049C>T (p.Thr350Ile)	rs200796750
NM_007078.3(LDB3):c.690-4A>G	rs45529531
NM_007078.3(LDB3):c.896+6722G>A	rs144445130

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