Variants in gene VLDLR with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 12

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HGVS	dbSNP
NM_003383.5(VLDLR):c.1162C>T (p.Leu388=)	rs114172780
NM_003383.5(VLDLR):c.1458C>T (p.Ala486=)	rs6143
NM_003383.5(VLDLR):c.175G>A (p.Val59Ile)	rs6149
NM_003383.5(VLDLR):c.1809C>T (p.Asn603=)	rs6147
NM_003383.5(VLDLR):c.242A>G (p.Asn81Ser)	rs140526335
NM_003383.5(VLDLR):c.24G>A (p.Ala8=)	rs34336270
NM_003383.5(VLDLR):c.464G>C (p.Ser155Thr)	rs34080096
NM_003383.5(VLDLR):c.468C>T (p.Pro156=)	rs2242105
NM_003383.5(VLDLR):c.738C>T (p.Cys246=)	rs116687040
NM_003383.5(VLDLR):c.75C>T (p.Thr25=)	rs532555108
NM_003383.5(VLDLR):c.944-5T>C	rs35782329
NM_003383.5(VLDLR):c.982A>G (p.Ser328Gly)	rs116306908

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