Variants in gene LTBP4 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely 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: 8

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HGVS	dbSNP
NM_003573.2(LTBP4):c.1328G>A (p.Gly443Asp)	rs114749335
NM_003573.2(LTBP4):c.1531A>G (p.Met511Val)	rs116005784
NM_003573.2(LTBP4):c.1581G>T (p.Arg527=)	rs117273116
NM_003573.2(LTBP4):c.2389+9A>G	rs73544980
NM_003573.2(LTBP4):c.2526G>A (p.Val842=)	rs371083223
NM_003573.2(LTBP4):c.2771-10C>G	rs200914063
NM_003573.2(LTBP4):c.2999C>G (p.Pro1000Arg)	rs200667255
NM_003573.2(LTBP4):c.79C>T (p.Leu27=)	rs370696272

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