ClinVar Miner

List of variants in gene LRP5 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_002335.4(LRP5):c.2092-194G>A rs577056703 0.01817
NM_002335.4(LRP5):c.2091+200G>C rs148842122 0.01720
NM_002335.4(LRP5):c.4586+250C>T rs570947 0.01502
NM_002335.4(LRP5):c.4111+56G>A rs80008081 0.01491
NM_002335.4(LRP5):c.3637+163C>T rs79307835 0.01318
NM_002335.4(LRP5):c.1016-91T>C rs75721054 0.01314
NM_002335.4(LRP5):c.1413-184G>A rs115157584 0.01311
NM_002335.4(LRP5):c.4111+212G>A rs539600 0.01286
NM_002335.4(LRP5):c.3427+276C>T rs181883339 0.01278
NM_002335.4(LRP5):c.4489-239C>T rs142772908 0.01271
NM_002335.4(LRP5):c.1801+297G>A rs115928312 0.01236
NM_002335.4(LRP5):c.3236+52G>A rs141442559 0.01205
NM_002335.4(LRP5):c.4489-163T>G rs151071785 0.01183
NM_002335.4(LRP5):c.884-123C>T rs72932379 0.01172
NM_002335.4(LRP5):c.489-267G>A rs115042402 0.01075
NM_002335.4(LRP5):c.4349-318C>T rs35388122 0.01031
NM_002335.4(LRP5):c.3764-176G>A rs191381016 0.00898
NM_002335.4(LRP5):c.1802-86G>A rs114263115 0.00883
NM_002335.4(LRP5):c.4587-222A>G rs139206235 0.00840
NM_002335.4(LRP5):c.883+206G>A rs150783920 0.00837
NM_002335.4(LRP5):c.3236+63C>T rs117846514 0.00757
NM_002335.4(LRP5):c.3428-179C>T rs116934080 0.00751
NM_002335.4(LRP5):c.687-17C>T rs186410639 0.00751
NM_002335.4(LRP5):c.4587-140G>A rs111392797 0.00707
NM_002335.4(LRP5):c.92-95A>C rs142253047 0.00687
NM_002335.4(LRP5):c.2827+136G>A rs150366250 0.00650
NM_002335.4(LRP5):c.3428-142C>G rs191633500 0.00596
NM_002335.4(LRP5):c.1412+48C>A rs73513071 0.00515
NM_002335.4(LRP5):c.2504-239G>A rs75313391 0.00505
NM_002335.4(LRP5):c.2319-125G>A rs78943283 0.00504
NM_002335.4(LRP5):c.2091+147T>C rs567358189 0.00499
NM_002335.4(LRP5):c.1015+66G>A rs190498589 0.00479
NM_002335.4(LRP5):c.883+252A>G rs547143863 0.00450
NM_002335.4(LRP5):c.1413-169C>T rs73513074 0.00415
NM_002335.4(LRP5):c.3637+100G>A rs138678613 0.00379
NM_002335.4(LRP5):c.1584+184C>T rs79762316 0.00361
NM_002335.4(LRP5):c.4349-201T>C rs115974399 0.00342
NM_002335.4(LRP5):c.3237-166C>T rs74585752 0.00320
NM_002335.4(LRP5):c.4111+34C>T rs150137194 0.00312
NM_002335.4(LRP5):c.4587-32G>A rs143336071 0.00292
NM_002335.4(LRP5):c.4431C>T (p.His1477=) rs11574426 0.00238
NM_002335.4(LRP5):c.2124G>A (p.Ser708=) rs140977837 0.00230
NM_002335.4(LRP5):c.4209C>G (p.Val1403=) rs147671915 0.00226
NM_002335.4(LRP5):c.3107G>A (p.Arg1036Gln) rs61889560 0.00207
NM_002335.4(LRP5):c.4089C>T (p.Asp1363=) rs3736229 0.00195
NM_002335.4(LRP5):c.1968C>T (p.His656=) rs144847027 0.00194
NM_002335.4(LRP5):c.4380C>T (p.Ser1460=) rs11574420 0.00182
NM_002335.4(LRP5):c.2295G>A (p.Ser765=) rs140955013 0.00156
NM_002335.4(LRP5):c.4623G>A (p.Thr1541=) rs139974816 0.00155
NM_002335.4(LRP5):c.3990G>A (p.Ala1330=) rs147637431 0.00108
NM_002335.4(LRP5):c.263A>G (p.Lys88Arg) rs78219242 0.00095
NM_002335.4(LRP5):c.4112-14T>C rs200717286 0.00078
NM_002335.4(LRP5):c.518C>T (p.Thr173Met) rs80358306 0.00049
NM_002335.4(LRP5):c.2445C>T (p.Asp815=) rs149080536 0.00046
NM_002335.4(LRP5):c.1585-9G>A rs202067798 0.00042
NM_002335.4(LRP5):c.1395A>C (p.Ala465=) rs200075657 0.00022
NM_002335.4(LRP5):c.3361A>G (p.Asn1121Asp) rs80358317 0.00021
NM_002335.4(LRP5):c.1299C>T (p.Thr433=) rs145362529 0.00016
NM_002335.4(LRP5):c.2766C>T (p.Gly922=) rs139372523 0.00016
NM_002335.4(LRP5):c.303C>T (p.Asn101=) rs372860842 0.00011
NM_002335.4(LRP5):c.4489-11G>T rs201761017 0.00004
NM_002335.4(LRP5):c.228C>T (p.Ala76=) rs564857130 0.00003
NM_002335.4(LRP5):c.4659C>T (p.Ser1553=) rs112415702 0.00002
NM_002335.4(LRP5):c.1585-11C>T rs1380761384 0.00001
NM_002335.4(LRP5):c.-19del rs763941232
NM_002335.4(LRP5):c.1801+351G>A rs78855542
NM_002335.4(LRP5):c.2092-137G>A rs149787603
NM_002335.4(LRP5):c.2092-49del rs371789773
NM_002335.4(LRP5):c.2828-264dup rs528947020
NM_002335.4(LRP5):c.3427+37C>T
NM_002335.4(LRP5):c.3428-270G>A rs141422727
NM_002335.4(LRP5):c.375G>T (p.Thr125=) rs780348578
NM_002335.4(LRP5):c.4112-319G>C rs139857216
NM_002335.4(LRP5):c.4489-162C>A rs140072262
NM_002335.4(LRP5):c.488+218G>T rs182387912

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