ClinVar Miner

List of variants in gene LRP5 reported as benign for not specified

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Gene type:
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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_002335.4(LRP5):c.1647T>C (p.Phe549=) rs545382 0.83202
NM_002335.4(LRP5):c.3357G>A (p.Val1119=) rs556442 0.55735
NM_002335.4(LRP5):c.884-4T>C rs314776 0.48379
NM_002335.4(LRP5):c.1412+8G>A rs4988319 0.15090
NM_002335.4(LRP5):c.2220C>T (p.Asn740=) rs2306862 0.11683
NM_002335.4(LRP5):c.3989C>T (p.Ala1330Val) rs3736228 0.10701
NM_002335.4(LRP5):c.2318+6T>C rs4988322 0.06393
NM_002335.4(LRP5):c.1932G>A (p.Glu644=) rs2277268 0.06342
NM_002335.4(LRP5):c.1999G>A (p.Val667Met) rs4988321 0.03472
NM_002335.4(LRP5):c.4000+10T>A rs116068042 0.02476
NM_002335.4(LRP5):c.3297C>T (p.Asp1099=) rs17149104 0.02225
NM_002335.4(LRP5):c.4788C>T (p.Thr1596=) rs113442867 0.01233
NM_002335.4(LRP5):c.3918G>A (p.Ala1306=) rs11574425 0.01064
NM_002335.4(LRP5):c.4574C>T (p.Ala1525Val) rs1127291 0.01003
NM_002335.4(LRP5):c.266A>G (p.Gln89Arg) rs41494349 0.00826
NM_002335.4(LRP5):c.3564G>A (p.Arg1188=) rs117289001 0.00762
NM_002335.4(LRP5):c.687-8G>A rs190810239 0.00718
NM_002335.4(LRP5):c.459G>A (p.Pro153=) rs78844574 0.00559
NM_002335.4(LRP5):c.4000+9C>T rs148685646 0.00389
NM_002335.4(LRP5):c.4635C>T (p.Thr1545=) rs145406397 0.00373
NM_002335.4(LRP5):c.2139G>A (p.Val713=) rs34369535 0.00322
NM_002335.4(LRP5):c.16C>A (p.Pro6Thr) rs771718186 0.00289
NM_002335.4(LRP5):c.4431C>T (p.His1477=) rs11574426 0.00238
NM_002335.4(LRP5):c.4209C>G (p.Val1403=) rs147671915 0.00226
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.1801+725G>A rs576510976 0.00128
NM_002335.4(LRP5):c.2193C>T (p.Asn731=) rs147388442 0.00108
NM_002335.4(LRP5):c.3723A>G (p.Pro1241=) rs139554243 0.00100
NM_002335.4(LRP5):c.1413-7T>A rs141889567 0.00077
NM_002335.4(LRP5):c.2445C>T (p.Asp815=) rs149080536 0.00046
NM_002335.4(LRP5):c.4511C>T (p.Pro1504Leu) rs201475647 0.00039
NM_002335.4(LRP5):c.675C>T (p.Asp225=) rs138207107 0.00031
NM_002335.4(LRP5):c.2115C>T (p.Asn705=) rs145456776 0.00017
NM_002335.4(LRP5):c.141C>T (p.Asp47=) rs375980894 0.00012
NM_002335.4(LRP5):c.2467C>T (p.Leu823=) rs768741253 0.00005
NM_002335.4(LRP5):c.1392C>T (p.Ile464=) rs569443429
NM_002335.4(LRP5):c.34CTG[10] (p.Leu20dup) rs72555376
NM_002335.4(LRP5):c.34CTG[8] (p.Leu20del) rs72555376
NM_002335.4(LRP5):c.4458G>T (p.Ser1486=) rs75571306
NM_002335.4(LRP5):c.4614C>T (p.Pro1538=) rs1421178463

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