ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 18
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HGVS dbSNP gnomAD frequency
NM_003383.5(VLDLR):c.2416+8G>T rs6145 0.24562
NM_003383.5(VLDLR):c.1187-3C>T rs11789583 0.15129
NM_003383.5(VLDLR):c.2067A>G (p.Gln689=) rs6148 0.13882
NM_003383.5(VLDLR):c.175G>A (p.Val59Ile) rs6149 0.05632
NM_003383.5(VLDLR):c.944-5T>C rs35782329 0.03136
NM_003383.5(VLDLR):c.464G>C (p.Ser155Thr) rs34080096 0.00311
NM_003383.5(VLDLR):c.982A>G (p.Ser328Gly) rs116306908 0.00238
NM_003383.5(VLDLR):c.2291C>T (p.Thr764Met) rs56737058 0.00223
NM_003383.5(VLDLR):c.1485-12A>G rs146156696 0.00163
NM_003383.5(VLDLR):c.1162C>T (p.Leu388=) rs114172780 0.00146
NM_003383.5(VLDLR):c.1074C>T (p.Asn358=) rs115059319 0.00116
NM_003383.5(VLDLR):c.242A>G (p.Asn81Ser) rs140526335 0.00115
NM_003383.5(VLDLR):c.1809C>T (p.Asn603=) rs6147 0.00088
NM_003383.5(VLDLR):c.943+19T>C rs144551353 0.00078
NM_003383.5(VLDLR):c.468C>T (p.Pro156=) rs2242105 0.00058
NM_003383.5(VLDLR):c.954C>T (p.Cys318=) rs373943845 0.00026
NM_003383.5(VLDLR):c.738C>T (p.Cys246=) rs116687040 0.00020
NM_003383.5(VLDLR):c.-42GGC[9] rs71329437

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