ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
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.4278T>C (p.Tyr1426=) rs142328132 0.00250
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.1968C>T (p.His656=) rs144847027 0.00194
NM_002335.4(LRP5):c.1801+675A>G rs555106014 0.00188
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.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.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.1738G>A (p.Val580Ile) rs149524398 0.00024
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.4029T>C (p.Cys1343=) rs138359428 0.00009
NM_002335.4(LRP5):c.3018C>T (p.Asp1006=) rs146792434 0.00004
NM_002335.4(LRP5):c.2079C>T (p.Asp693=) rs770364888 0.00001
NM_002335.4(LRP5):c.2760C>T (p.Ile920=) rs2098661060 0.00001
NM_002335.4(LRP5):c.3228G>A (p.Ala1076=) rs767509386 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.3015C>T (p.Asp1005=)
NM_002335.4(LRP5):c.3091A>G (p.Ile1031Val)
NM_002335.4(LRP5):c.3330C>A (p.Gly1110=)
NM_002335.4(LRP5):c.34CTG[6] (p.Leu18_Leu20del) rs72555376
NM_002335.4(LRP5):c.3768G>A (p.Pro1256=) rs746916192
NM_002335.4(LRP5):c.4134C>T (p.Asp1378=)
NM_002335.4(LRP5):c.4446G>C (p.Ser1482=) rs142191419
NM_002335.4(LRP5):c.915C>G (p.Gly305=) rs1591232305
NM_002335.4(LRP5):c.943A>G (p.Ser315Gly)

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