ClinVar Miner

List of variants in gene LRP2 studied for not specified

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Gene type:
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Total variants: 104
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HGVS dbSNP gnomAD frequency
NM_004525.3(LRP2):c.63G>C (p.Ala21=) rs1559014 0.99771
NM_004525.3(LRP2):c.79+15A>G rs1559013 0.98894
NM_004525.3(LRP2):c.12280A>G (p.Lys4094Glu) rs2075252 0.79497
NM_004525.3(LRP2):c.2025C>T (p.Val675=) rs830994 0.61350
NM_004525.3(LRP2):c.12628A>C (p.Ile4210Leu) rs4667591 0.60691
NM_004525.3(LRP2):c.13113C>T (p.Ile4371=) rs990626 0.59977
NM_004525.3(LRP2):c.2460A>G (p.Thr820=) rs2241190 0.54408
NM_004525.3(LRP2):c.3069A>G (p.Thr1023=) rs831043 0.53755
NM_004525.3(LRP2):c.3550+14C>T rs2075254 0.53578
NM_004525.3(LRP2):c.3667+20A>C rs831041 0.52466
NM_004525.3(LRP2):c.3660A>G (p.Ala1220=) rs831042 0.50520
NM_004525.3(LRP2):c.10503G>A (p.Gln3501=) rs2229265 0.45093
NM_004525.3(LRP2):c.3054C>A (p.Thr1018=) rs2075249 0.41290
NM_004525.3(LRP2):c.4875T>C (p.Cys1625=) rs2229267 0.38704
NM_004525.3(LRP2):c.4294+19C>T rs830973 0.35398
NM_004525.3(LRP2):c.248A>G (p.Asn83Ser) rs2229263 0.33289
NM_004525.3(LRP2):c.639C>T (p.Asp213=) rs2229266 0.30270
NM_004525.3(LRP2):c.8614G>A (p.Ala2872Thr) rs2228171 0.25207
NM_004525.3(LRP2):c.5100C>T (p.Ser1700=) rs2302694 0.19156
NM_004525.3(LRP2):c.5859A>G (p.Arg1953=) rs11886219 0.16510
NM_004525.3(LRP2):c.11601T>C (p.Cys3867=) rs2229268 0.15380
NM_004525.3(LRP2):c.7626C>G (p.Arg2542=) rs13397109 0.12249
NM_004525.3(LRP2):c.2376T>C (p.Asp792=) rs33954745 0.09210
NM_004525.3(LRP2):c.769+18T>C rs62171262 0.05350
NM_004525.3(LRP2):c.6759T>C (p.Asp2253=) rs35114151 0.04805
NM_004525.3(LRP2):c.4236G>C (p.Arg1412=) rs34915742 0.04398
NM_004525.3(LRP2):c.4046-6T>C rs76714416 0.04392
NM_004525.3(LRP2):c.13155C>T (p.His4385=) rs16856476 0.04079
NM_004525.3(LRP2):c.3836A>C (p.Asp1279Ala) rs17848149 0.03848
NM_004525.3(LRP2):c.7894A>G (p.Asn2632Asp) rs17848169 0.02788
NM_004525.3(LRP2):c.12151+4T>C rs17848192 0.02665
NM_004525.3(LRP2):c.2006G>A (p.Gly669Asp) rs34291900 0.02496
NM_004525.3(LRP2):c.6045C>T (p.Ala2015=) rs34834388 0.01962
NM_004525.3(LRP2):c.4344C>G (p.Ala1448=) rs35297090 0.01784
NM_004525.3(LRP2):c.6035G>A (p.Arg2012Lys) rs4667596 0.01732
NM_004525.3(LRP2):c.11759-5T>G rs76488092 0.01524
NM_004525.3(LRP2):c.3452C>T (p.Pro1151Leu) rs150552608 0.01319
NM_004525.3(LRP2):c.7253A>G (p.Glu2418Gly) rs61995915 0.01278
NM_004525.3(LRP2):c.13250G>A (p.Gly4417Asp) rs41268685 0.01191
NM_004525.3(LRP2):c.13134C>G (p.Pro4378=) rs73970129 0.01063
NM_004525.3(LRP2):c.10804G>A (p.Ala3602Thr) rs144081819 0.01045
NM_004525.3(LRP2):c.5293G>A (p.Val1765Met) rs116456291 0.01031
NM_004525.3(LRP2):c.9033-8T>C rs140148483 0.01021
NM_004525.3(LRP2):c.5085G>A (p.Ser1695=) rs145384264 0.00999
NM_004525.3(LRP2):c.1172-8G>A rs115371758 0.00955
NM_004525.3(LRP2):c.1167T>G (p.Asp389Glu) rs111704488 0.00952
NM_004525.3(LRP2):c.11996T>G (p.Val3999Gly) rs79723119 0.00834
NM_004525.3(LRP2):c.2175C>T (p.Thr725=) rs141180155 0.00820
NM_004525.3(LRP2):c.13803G>A (p.Met4601Ile) rs34564141 0.00790
NM_004525.3(LRP2):c.10403C>T (p.Pro3468Leu) rs143367996 0.00734
NM_004525.3(LRP2):c.923-6G>A rs144147038 0.00611
NM_004525.3(LRP2):c.11092G>A (p.Val3698Met) rs34355135 0.00560
NM_004525.3(LRP2):c.8892G>A (p.Arg2964=) rs149148763 0.00557
NM_004525.3(LRP2):c.3659C>T (p.Ala1220Val) rs144723964 0.00467
NM_004525.3(LRP2):c.9613A>G (p.Asn3205Asp) rs35734447 0.00426
NM_004525.3(LRP2):c.6194T>C (p.Ile2065Thr) rs2228168 0.00369
NM_004525.3(LRP2):c.2933C>T (p.Thr978Met) rs114842875 0.00322
NM_004525.3(LRP2):c.92C>T (p.Ala31Val) rs144829356 0.00280
NM_004525.3(LRP2):c.769+9G>A rs148452352 0.00225
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.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.9914G>A (p.Arg3305His) rs3213760 0.00150
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.5209C>T (p.Leu1737Phe) rs149469954 0.00126
NM_004525.3(LRP2):c.2603C>G (p.Thr868Ser) rs150752263 0.00100
NM_004525.3(LRP2):c.987G>A (p.Ala329=) rs141751667 0.00084
NM_004525.3(LRP2):c.3311A>G (p.His1104Arg) rs144906000 0.00073
NM_004525.3(LRP2):c.10165A>G (p.Ile3389Val) rs140272085 0.00055
NM_004525.3(LRP2):c.13610A>C (p.Gln4537Pro) rs188918037 0.00049
NM_004525.3(LRP2):c.2511C>T (p.Ala837=) rs375313914 0.00034
NM_004525.3(LRP2):c.5107C>T (p.Pro1703Ser) rs141260047 0.00024
NM_004525.3(LRP2):c.9040C>T (p.Arg3014Trp) rs142093111 0.00022
NM_004525.3(LRP2):c.4035C>T (p.Ser1345=) rs200587303 0.00021
NM_004525.3(LRP2):c.8169C>T (p.Asn2723=) rs200369596 0.00011
NM_004525.3(LRP2):c.12296-4G>A rs375166826 0.00009
NM_004525.3(LRP2):c.11461G>A (p.Ala3821Thr) rs778317120 0.00005
NM_004525.3(LRP2):c.2485C>T (p.Arg829Trp) rs368619363 0.00004
NM_004525.3(LRP2):c.13847C>T (p.Ser4616Leu) rs140802648 0.00002
NM_004525.3(LRP2):c.39C>T (p.Leu13=) rs529649802 0.00002
NM_004525.3(LRP2):c.8141C>T (p.Ser2714Leu) rs774369141 0.00002
NM_004525.3(LRP2):c.10697C>G (p.Thr3566Ser) rs756870198 0.00001
NM_004525.3(LRP2):c.1742T>C (p.Ile581Thr) rs779652105 0.00001
NM_004525.3(LRP2):c.4855C>A (p.Leu1619Ile) rs766931921 0.00001
NM_004525.3(LRP2):c.5626A>G (p.Ile1876Val) rs763254934 0.00001
NM_004525.3(LRP2):c.6442C>T (p.Arg2148Trp) rs774074912 0.00001
NM_004525.3(LRP2):c.8372G>A (p.Arg2791Lys) rs139266058 0.00001
NM_004525.3(LRP2):c.1018C>G (p.His340Asp) rs777908550
NM_004525.3(LRP2):c.10654T>G (p.Phe3552Val) rs2105284304
NM_004525.3(LRP2):c.11498-13del rs143342962
NM_004525.3(LRP2):c.3157G>A (p.Asp1053Asn) rs1432929481
NM_004525.3(LRP2):c.3550+18T>G rs2075255
NM_004525.3(LRP2):c.3973T>C (p.Cys1325Arg) rs797045683
NM_004525.3(LRP2):c.402C>A (p.Pro134=) rs34104660
NM_004525.3(LRP2):c.428-9_428-8del rs370823033
NM_004525.3(LRP2):c.4733G>A (p.Arg1578His)
NM_004525.3(LRP2):c.4866G>A (p.Met1622Ile) rs2105375209
NM_004525.3(LRP2):c.770-4dup
NM_004525.3(LRP2):c.7715+3A>T rs797045684
NM_004525.3(LRP2):c.775G>C (p.Gly259Arg) rs34693334
NM_004525.3(LRP2):c.8579C>T (p.Thr2860Ile) rs765920078

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