ClinVar Miner

List of variants in gene LAMP2 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_002294.3(LAMP2):c.156A>T (p.Val52=) rs12097 0.39324
NM_002294.3(LAMP2):c.*297A>C rs8160 0.09815
NM_002294.3(LAMP2):c.*3248G>A rs5957380 0.09812
NM_002294.3(LAMP2):c.*486A>G rs5957383 0.09784
NM_002294.3(LAMP2):c.927C>T (p.Ser309=) rs73219144 0.02702
NM_002294.3(LAMP2):c.*205C>T rs41300191 0.02502
NM_002294.3(LAMP2):c.*2746A>G rs3827478 0.01396
NM_002294.3(LAMP2):c.1094-140A>G rs141348126 0.01356
NM_002294.3(LAMP2):c.929-126G>A rs7888393 0.01266
NM_002294.3(LAMP2):c.*2162G>A rs767123866 0.01199
NM_002294.3(LAMP2):c.*3249T>C rs41300908 0.01188
NM_002294.3(LAMP2):c.865-242C>A rs146283621 0.01021
NM_002294.3(LAMP2):c.741+224C>T rs181256167 0.01012
NM_002294.3(LAMP2):c.1094-322G>A rs57800983 0.00828
NM_002294.3(LAMP2):c.*3459G>T rs185990694 0.00648
NM_002294.3(LAMP2):c.*237C>T rs143070918 0.00627
NM_002294.3(LAMP2):c.929-292G>A rs185059445 0.00492
NM_002294.3(LAMP2):c.865-310C>T rs181144328 0.00480
NM_002294.3(LAMP2):c.*1984G>A rs148513908 0.00454
NM_002294.3(LAMP2):c.1093+2514G>A rs144140265 0.00404
NM_002294.3(LAMP2):c.65-58T>A rs192733755 0.00307
NM_002294.3(LAMP2):c.661G>A (p.Gly221Arg) rs145169006 0.00193
NM_002294.3(LAMP2):c.755T>G (p.Ile252Ser) rs141541387 0.00119
NM_002294.3(LAMP2):c.864+83G>A rs768677322 0.00113
NM_002294.3(LAMP2):c.*4963del rs754879365 0.00097
NM_002294.3(LAMP2):c.*853G>A rs763861761 0.00088
NM_002294.3(LAMP2):c.*1413A>G rs773379092 0.00076
NM_002294.3(LAMP2):c.339C>T (p.Ser113=) rs147369153 0.00066
NM_002294.3(LAMP2):c.*4757A>G rs767652057 0.00040
NM_002294.3(LAMP2):c.*4961A>G rs765371462 0.00039
NM_002294.3(LAMP2):c.586A>T (p.Thr196Ser) rs138991195 0.00039
NM_002294.3(LAMP2):c.741+11C>T rs149155417 0.00024
NM_002294.3(LAMP2):c.1093+2478A>G rs140936359 0.00014
NM_002294.3(LAMP2):c.591G>A (p.Val197=) rs201030806 0.00014
NM_002294.3(LAMP2):c.1093+2485T>C rs1301008847 0.00012
NM_002294.3(LAMP2):c.1093+2544A>G rs777128122 0.00009
NM_002294.3(LAMP2):c.157C>T (p.Arg53Cys) rs752321157 0.00009
NM_002294.3(LAMP2):c.42C>T (p.Leu14=) rs727503122 0.00009
NM_002294.3(LAMP2):c.*2794T>C rs368937075 0.00008
NM_002294.3(LAMP2):c.*2678G>A rs775547188 0.00006
NM_002294.3(LAMP2):c.*2771A>G rs747304113 0.00004
NM_002294.3(LAMP2):c.299C>T (p.Ala100Val) rs397516741 0.00004
NM_002294.3(LAMP2):c.517G>A (p.Val173Ile) rs141574558 0.00004
NM_002294.3(LAMP2):c.929-5T>C rs375341409 0.00004
NM_002294.3(LAMP2):c.300G>A (p.Ala100=) rs765548221 0.00003
NM_002294.3(LAMP2):c.398-3T>C rs1045629648 0.00003
NM_002294.3(LAMP2):c.519A>G (p.Val173=) rs1060504543 0.00003
NM_002294.3(LAMP2):c.65-20A>T rs773064698 0.00003
NM_002294.3(LAMP2):c.929-29A>G rs773549757 0.00003
NM_002294.3(LAMP2):c.340G>A (p.Val114Ile) rs377652722 0.00002
NM_002294.3(LAMP2):c.797G>A (p.Arg266His) rs200934351 0.00002
NM_002294.3(LAMP2):c.*2755G>C rs1274595954 0.00001
NM_002294.3(LAMP2):c.1139C>T (p.Ala380Val) rs747301460 0.00001
NM_002294.3(LAMP2):c.209G>T (p.Gly70Val) rs1340367353 0.00001
NM_002294.3(LAMP2):c.398-5T>C rs1460188868 0.00001
NM_001122606.1(LAMP2):c.1094-549AT[11] rs753399289
NM_002294.3(LAMP2):c.*1243A>G rs147825361
NM_002294.3(LAMP2):c.*1673G>T
NM_002294.3(LAMP2):c.*2136GT[7] rs1556075606
NM_002294.3(LAMP2):c.*2147_*2148insGTATAT rs778330920
NM_002294.3(LAMP2):c.*2213TATATATACACA[1] rs200167553
NM_002294.3(LAMP2):c.*3347GTTA[1] rs764018077
NM_002294.3(LAMP2):c.*3459GTT[3] rs199705754
NM_002294.3(LAMP2):c.-23_-16del rs1556124290
NM_002294.3(LAMP2):c.-32GTCGCCGCC[1] rs193922648
NM_002294.3(LAMP2):c.-32GTCGCCGCC[3] rs193922648
NM_002294.3(LAMP2):c.-4G>C rs200297370
NM_002294.3(LAMP2):c.449T>A (p.Leu150His)
NM_002294.3(LAMP2):c.46C>T (p.Leu16=)
NM_002294.3(LAMP2):c.557-128dup rs775935754
NM_002294.3(LAMP2):c.557-251G>T rs148242561
NM_002294.3(LAMP2):c.742-7_742-5del rs779710402
NM_002294.3(LAMP2):c.865-311G>T rs185635351
NM_002294.3(LAMP2):c.865-8del rs746330494

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