ClinVar Miner

List of variants in gene LRP2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_004525.3(LRP2):c.2006G>A (p.Gly669Asp) rs34291900 0.02496
NM_004525.3(LRP2):c.5085G>A (p.Ser1695=) rs145384264 0.00999
NM_004525.3(LRP2):c.2175C>T (p.Thr725=) rs141180155 0.00820
NM_004525.3(LRP2):c.923-6G>A rs144147038 0.00611
NM_004525.3(LRP2):c.1502G>A (p.Arg501Gln) rs138705366 0.00218
NM_004525.3(LRP2):c.12379C>A (p.Arg4127Ser) rs148356370 0.00217
NM_004525.3(LRP2):c.13685T>C (p.Val4562Ala) rs142245618 0.00201
NM_004525.3(LRP2):c.10030G>A (p.Ala3344Thr) rs137983840 0.00185
NM_004525.3(LRP2):c.12725A>G (p.Asp4242Gly) rs35942532 0.00171
NM_004525.3(LRP2):c.3122A>G (p.Asn1041Ser) rs143028579 0.00170
NM_004525.3(LRP2):c.4351G>T (p.Val1451Phe) rs146289506 0.00164
NM_004525.3(LRP2):c.6473A>C (p.Asn2158Thr) rs34052957 0.00157
NM_004525.3(LRP2):c.6954C>T (p.Asp2318=) rs34223099 0.00155
NM_004525.3(LRP2):c.9477G>A (p.Met3159Ile) rs144322413 0.00152
NM_004525.3(LRP2):c.13902C>G (p.Thr4634=) rs112043518 0.00145
NM_004525.3(LRP2):c.13935C>T (p.Thr4645=) rs150373759 0.00144
NM_004525.3(LRP2):c.7406A>G (p.Asp2469Gly) rs116507519 0.00143
NM_004525.3(LRP2):c.2178G>T (p.Leu726Phe) rs144451000 0.00139
NM_004525.3(LRP2):c.3110G>A (p.Arg1037Lys) rs147058423 0.00133
NM_004525.3(LRP2):c.12287T>C (p.Ile4096Thr) rs137922929 0.00129
NM_004525.3(LRP2):c.13921A>T (p.Thr4641Ser) rs79179577 0.00123
NM_004525.3(LRP2):c.3100A>G (p.Lys1034Glu) rs150395163 0.00120
NM_004525.3(LRP2):c.391A>G (p.Arg131Gly) rs34592807 0.00109
NM_004525.3(LRP2):c.2603C>G (p.Thr868Ser) rs150752263 0.00100
NM_004525.3(LRP2):c.6176C>T (p.Ser2059Phe) rs148299415 0.00098
NM_004525.3(LRP2):c.11870C>T (p.Ser3957Phe) rs143400476 0.00091
NM_004525.3(LRP2):c.9650A>G (p.Tyr3217Cys) rs143150497 0.00083
NM_004525.3(LRP2):c.299G>A (p.Arg100His) rs35642533 0.00081
NM_004525.3(LRP2):c.8070G>A (p.Lys2690=) rs144284604 0.00078
NM_004525.3(LRP2):c.1176C>T (p.Gly392=) rs369145798 0.00070
NM_004525.3(LRP2):c.6938C>T (p.Pro2313Leu) rs73035708 0.00069
NM_004525.3(LRP2):c.7926T>G (p.Thr2642=) rs138903794 0.00063
NM_004525.3(LRP2):c.4928G>A (p.Arg1643Gln) rs147688332 0.00059
NM_004525.3(LRP2):c.12420C>T (p.Tyr4140=) rs34663643 0.00053
NM_004525.3(LRP2):c.7866C>T (p.Asp2622=) rs139514301 0.00047
NM_004525.3(LRP2):c.6553C>T (p.Leu2185Phe) rs143884041 0.00043
NM_004525.3(LRP2):c.10536C>T (p.Cys3512=) rs531013104 0.00039
NM_004525.3(LRP2):c.3551-9C>A rs373882047 0.00030
NM_004525.3(LRP2):c.8505T>C (p.Cys2835=) rs140925226 0.00027
NM_004525.3(LRP2):c.8529C>T (p.Asp2843=) rs144486598 0.00025
NM_004525.3(LRP2):c.4035C>T (p.Ser1345=) rs200587303 0.00021
NM_004525.3(LRP2):c.6130G>A (p.Ala2044Thr) rs142266106 0.00021
NM_004525.3(LRP2):c.11478G>A (p.Ala3826=) rs150464677 0.00019
NM_004525.3(LRP2):c.8073C>T (p.His2691=) rs146772976 0.00018
NM_004525.3(LRP2):c.12687T>C (p.Gly4229=) rs140195786 0.00016
NM_004525.3(LRP2):c.12243G>A (p.Glu4081=) rs371277503 0.00014
NM_004525.3(LRP2):c.7296A>G (p.Arg2432=) rs370035430 0.00014
NM_004525.3(LRP2):c.13353C>T (p.Thr4451=) rs767379633 0.00013
NM_004525.3(LRP2):c.2193T>C (p.Asp731=) rs539460153 0.00013
NM_004525.3(LRP2):c.5370A>G (p.Gln1790=) rs201155152 0.00011
NM_004525.3(LRP2):c.8112C>A (p.Ser2704=) rs148473513 0.00010
NM_004525.3(LRP2):c.9066C>T (p.Ser3022=) rs374380173 0.00010
NM_004525.3(LRP2):c.13326T>C (p.Ile4442=) rs141160195 0.00009
NM_004525.3(LRP2):c.3306C>A (p.Pro1102=) rs200584347 0.00009
NM_004525.3(LRP2):c.6106G>A (p.Val2036Ile) rs34041086 0.00009
NM_004525.3(LRP2):c.11888-10T>C rs199803112 0.00008
NM_004525.3(LRP2):c.3333C>T (p.Asp1111=) rs372322747 0.00008
NM_004525.3(LRP2):c.7586A>G (p.His2529Arg) rs139696516 0.00008
NM_004525.3(LRP2):c.11925C>T (p.Cys3975=) rs143815721 0.00007
NM_004525.3(LRP2):c.1425C>T (p.Asp475=) rs186484839 0.00007
NM_004525.3(LRP2):c.11380+7G>C rs201291642 0.00006
NM_004525.3(LRP2):c.2886G>C (p.Ser962=) rs138299719 0.00006
NM_004525.3(LRP2):c.2916C>T (p.Asn972=) rs142290901 0.00006
NM_004525.3(LRP2):c.4092T>C (p.Cys1364=) rs200311104 0.00006
NM_004525.3(LRP2):c.630C>T (p.Asp210=) rs368336310 0.00006
NM_004525.3(LRP2):c.5367G>A (p.Glu1789=) rs528249827 0.00005
NM_004525.3(LRP2):c.593G>A (p.Arg198His) rs372596334 0.00005
NM_004525.3(LRP2):c.8300G>A (p.Gly2767Asp) rs138382534 0.00004
NM_004525.3(LRP2):c.5535C>A (p.Ile1845=) rs772030872 0.00003
NM_004525.3(LRP2):c.13881G>A (p.Ser4627=) rs144292380 0.00002
NM_004525.3(LRP2):c.2639+7A>G rs776885594 0.00002
NM_004525.3(LRP2):c.39C>T (p.Leu13=) rs529649802 0.00002
NM_004525.3(LRP2):c.11145G>A (p.Glu3715=) rs769966400 0.00001
NM_004525.3(LRP2):c.11592T>C (p.Asp3864=) rs1184513457 0.00001
NM_004525.3(LRP2):c.12989-9G>A rs752178785 0.00001
NM_004525.3(LRP2):c.1827A>G (p.Leu609=) rs186137585 0.00001
NM_004525.3(LRP2):c.5867T>G (p.Leu1956Arg) rs756470766 0.00001
NM_004525.3(LRP2):c.11712T>C (p.Asn3904=)
NM_004525.3(LRP2):c.11961T>C (p.Phe3987=)
NM_004525.3(LRP2):c.12954T>G (p.Val4318=) rs1478283354
NM_004525.3(LRP2):c.1773-3C>T
NM_004525.3(LRP2):c.1794C>T (p.Gly598=)
NM_004525.3(LRP2):c.1986G>A (p.Pro662=)
NM_004525.3(LRP2):c.2694C>T (p.Thr898=)
NM_004525.3(LRP2):c.310+7G>A
NM_004525.3(LRP2):c.3190+10T>C
NM_004525.3(LRP2):c.3201T>C (p.Cys1067=)
NM_004525.3(LRP2):c.3678T>G (p.Pro1226=)
NM_004525.3(LRP2):c.387C>T (p.His129=)
NM_004525.3(LRP2):c.428-6C>A
NM_004525.3(LRP2):c.5052A>G (p.Gln1684=) rs568387449
NM_004525.3(LRP2):c.5466T>G (p.Pro1822=) rs775020369
NM_004525.3(LRP2):c.770-5C>T rs180797349
NM_004525.3(LRP2):c.8112C>T (p.Ser2704=)
NM_004525.3(LRP2):c.8526T>C (p.Cys2842=)
NM_004525.3(LRP2):c.8670T>C (p.Phe2890=)
NM_004525.3(LRP2):c.8853C>A (p.Ser2951=)
NM_004525.3(LRP2):c.923-3T>C
NM_004525.3(LRP2):c.9738A>G (p.Thr3246=) rs1574108633
NM_004525.3(LRP2):c.9894C>T (p.Asp3298=) rs2105296050

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