ClinVar Miner

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:
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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