ClinVar Miner

List of variants in gene VLDLR reported as uncertain significance by GeneDx

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_003383.5(VLDLR):c.982A>G (p.Ser328Gly) rs116306908 0.00238
NM_003383.5(VLDLR):c.1901G>A (p.Arg634His) rs35339834 0.00108
NM_003383.5(VLDLR):c.2371G>A (p.Val791Ile) rs35334949 0.00051
NM_003383.5(VLDLR):c.792C>T (p.Cys264=) rs141850403 0.00036
NM_003383.5(VLDLR):c.1297G>A (p.Val433Met) rs140062795 0.00026
NM_003383.5(VLDLR):c.1532A>G (p.Asn511Ser) rs182216426 0.00026
NM_003383.5(VLDLR):c.1132T>C (p.Tyr378His) rs142885301 0.00021
NM_003383.5(VLDLR):c.1948C>G (p.Leu650Val) rs116047052 0.00019
NM_003383.5(VLDLR):c.1838G>A (p.Arg613His) rs35948251 0.00017
NM_003383.5(VLDLR):c.340C>T (p.Arg114Cys) rs369746738 0.00015
NM_003383.5(VLDLR):c.836G>A (p.Arg279Gln) rs114307467 0.00014
NM_003383.5(VLDLR):c.1646T>A (p.Phe549Tyr) rs370936675 0.00012
NM_003383.5(VLDLR):c.104C>T (p.Pro35Leu) rs113809568 0.00007
NM_003383.5(VLDLR):c.569C>T (p.Pro190Leu) rs772075122 0.00007
NM_003383.5(VLDLR):c.140C>T (p.Thr47Met) rs763801214 0.00001
NM_003383.5(VLDLR):c.829A>C (p.Thr277Pro) rs1021503222 0.00001
NM_003383.5(VLDLR):c.922G>A (p.Asp308Asn) rs748931860 0.00001
NM_003383.5(VLDLR):c.1452C>A (p.Phe484Leu) rs144724569
NM_003383.5(VLDLR):c.1534G>A (p.Val512Ile)
NM_003383.5(VLDLR):c.1790C>T (p.Ala597Val)
NM_003383.5(VLDLR):c.217G>A (p.Ala73Thr)
NM_003383.5(VLDLR):c.2204C>G (p.Ser735Cys) rs745998932
NM_003383.5(VLDLR):c.232G>A (p.Val78Met) rs367862086
NM_003383.5(VLDLR):c.2524G>A (p.Glu842Lys) rs2130810779
NM_003383.5(VLDLR):c.467C>A (p.Pro156His) rs1554620955
NM_003383.5(VLDLR):c.611C>T (p.Ser204Phe) rs2130791427
NM_003383.5(VLDLR):c.827G>C (p.Arg276Pro) rs748580464

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