ClinVar Miner

List of variants in gene LRP5 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_002335.4(LRP5):c.4574C>T (p.Ala1525Val) rs1127291 0.01003
NM_002335.4(LRP5):c.3564G>A (p.Arg1188=) rs117289001 0.00762
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.4431C>T (p.His1477=) rs11574426 0.00238
NM_002335.4(LRP5):c.3107G>A (p.Arg1036Gln) rs61889560 0.00207
NM_002335.4(LRP5):c.1801+675A>G rs555106014 0.00188
NM_002335.4(LRP5):c.2295G>A (p.Ser765=) rs140955013 0.00156
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.2234C>T (p.Ala745Val) rs148550774 0.00083
NM_002335.4(LRP5):c.1413-7T>A rs141889567 0.00077
NM_002335.4(LRP5):c.291C>T (p.Ala97=) rs146667935 0.00061
NM_002335.4(LRP5):c.2445C>T (p.Asp815=) rs149080536 0.00046
NM_002335.4(LRP5):c.2829G>A (p.Pro943=) rs201018263 0.00046
NM_002335.4(LRP5):c.2763C>T (p.Pro921=) rs147158768 0.00039
NM_002335.4(LRP5):c.3403C>T (p.Arg1135Cys) rs143396225 0.00032
NM_002335.4(LRP5):c.639C>T (p.Asp213=) rs150859573 0.00022
NM_002335.4(LRP5):c.2358C>T (p.Ile786=) rs140616444 0.00019
NM_002335.4(LRP5):c.2724C>G (p.His908Gln) rs143539498 0.00011
NM_002335.4(LRP5):c.3245A>G (p.Tyr1082Cys) rs113804402 0.00011
NM_002335.4(LRP5):c.4029T>C (p.Cys1343=) rs138359428 0.00009
NM_002335.4(LRP5):c.1328C>T (p.Thr443Met) rs200416179 0.00007
NM_002335.4(LRP5):c.3655C>T (p.Arg1219Cys) rs139847357 0.00007
NM_002335.4(LRP5):c.3436C>T (p.Arg1146Cys) rs367862196 0.00004
NM_002335.4(LRP5):c.1613G>A (p.Arg538Gln) rs138692892 0.00003
NM_002335.4(LRP5):c.523C>T (p.Arg175Trp) rs373823574 0.00003
NM_002335.4(LRP5):c.1021G>A (p.Glu341Lys) rs184945579 0.00001
NM_002335.4(LRP5):c.2051T>C (p.Val684Ala) rs1339222045 0.00001
NM_002335.4(LRP5):c.2760C>T (p.Ile920=) rs2098661060 0.00001
NM_002335.4(LRP5):c.4488+6G>T rs751829465 0.00001
NM_002335.4(LRP5):c.4734G>A (p.Thr1578=) rs781203252 0.00001
NM_002335.4(LRP5):c.-19del rs763941232
NM_002335.4(LRP5):c.1015G>A (p.Gly339Arg)
NM_002335.4(LRP5):c.1532A>C (p.Asp511Ala)
NM_002335.4(LRP5):c.1861dup (p.His621fs) rs1303970751
NM_002335.4(LRP5):c.22C>A (p.Pro8Thr)
NM_002335.4(LRP5):c.2457C>G (p.Tyr819Ter) rs1057519127
NM_002335.4(LRP5):c.2608C>T (p.Arg870Trp) rs769188092
NM_002335.4(LRP5):c.29_37dup (p.Leu12_Leu13insArgProLeu)
NM_002335.4(LRP5):c.3397C>A (p.Leu1133Met)
NM_002335.4(LRP5):c.3446T>A (p.Leu1149Gln) rs200389686
NM_002335.4(LRP5):c.34CTG[6] (p.Leu18_Leu20del) rs72555376
NM_002335.4(LRP5):c.3683G>C (p.Cys1228Ser) rs2098670820
NM_002335.4(LRP5):c.3768G>A (p.Pro1256=) rs746916192
NM_002335.4(LRP5):c.3985G>A (p.Glu1329Lys)
NM_002335.4(LRP5):c.4078G>A (p.Asp1360Asn)
NM_002335.4(LRP5):c.4349-1G>A rs2098677103
NM_002335.4(LRP5):c.4441_4445delinsTG (p.Ala1481_Ser1482delinsTrp)
NM_002335.4(LRP5):c.4446G>C (p.Ser1482=) rs142191419
NM_002335.4(LRP5):c.480del (p.Ala161fs) rs1057519126
NM_002335.4(LRP5):c.915C>G (p.Gly305=) rs1591232305

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