ClinVar Miner

List of variants in gene LRP5 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 99
Download table as spreadsheet
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.3297C>T (p.Asp1099=) rs17149104 0.02225
NM_002335.4(LRP5):c.4788C>T (p.Thr1596=) rs113442867 0.01233
NM_002335.4(LRP5):c.266A>G (p.Gln89Arg) rs41494349 0.00826
NM_002335.4(LRP5):c.4000+9C>T rs148685646 0.00389
NM_002335.4(LRP5):c.4278T>C (p.Tyr1426=) rs142328132 0.00250
NM_002335.4(LRP5):c.2124G>A (p.Ser708=) rs140977837 0.00230
NM_002335.4(LRP5):c.3256A>G (p.Met1086Val) rs145774832 0.00208
NM_002335.4(LRP5):c.1801+675A>G rs555106014 0.00188
NM_002335.4(LRP5):c.486C>T (p.His162=) rs191882942 0.00140
NM_002335.4(LRP5):c.1801+725G>A rs576510976 0.00128
NM_002335.4(LRP5):c.4195G>A (p.Val1399Ile) rs113315676 0.00097
NM_002335.4(LRP5):c.2544G>A (p.Pro848=) rs148271293 0.00083
NM_002335.4(LRP5):c.1413-7T>A rs141889567 0.00077
NM_002335.4(LRP5):c.2637C>T (p.Arg879=) rs141174027 0.00069
NM_002335.4(LRP5):c.1032G>C (p.Leu344=) rs143499301 0.00050
NM_002335.4(LRP5):c.2445C>T (p.Asp815=) rs149080536 0.00046
NM_002335.4(LRP5):c.144C>T (p.Ala48=) rs776920568 0.00036
NM_002335.4(LRP5):c.3403C>T (p.Arg1135Cys) rs143396225 0.00032
NM_002335.4(LRP5):c.2503+10G>A rs191125304 0.00031
NM_002335.4(LRP5):c.2091+5C>T rs202064462 0.00021
NM_002335.4(LRP5):c.3879G>A (p.Glu1293=) rs759175453 0.00021
NM_002335.4(LRP5):c.4077C>T (p.Pro1359=) rs143482432 0.00019
NM_002335.4(LRP5):c.2115C>T (p.Asn705=) rs145456776 0.00017
NM_002335.4(LRP5):c.1833G>A (p.Gly611=) rs142126662 0.00014
NM_002335.4(LRP5):c.2175T>C (p.Val725=) rs200570645 0.00012
NM_002335.4(LRP5):c.303C>T (p.Asn101=) rs372860842 0.00011
NM_002335.4(LRP5):c.3837C>T (p.Arg1279=) rs372930578 0.00011
NM_002335.4(LRP5):c.4488+10G>A rs202206612 0.00010
NM_002335.4(LRP5):c.2883G>A (p.Pro961=) rs150031686 0.00009
NM_002335.4(LRP5):c.4029T>C (p.Cys1343=) rs138359428 0.00009
NM_002335.4(LRP5):c.4391T>C (p.Met1464Thr) rs113007633 0.00009
NM_002335.4(LRP5):c.3901G>A (p.Ala1301Thr) rs149166384 0.00008
NM_002335.4(LRP5):c.1518C>T (p.Asn506=) rs148073961 0.00007
NM_002335.4(LRP5):c.1077G>A (p.Thr359=) rs200179967 0.00006
NM_002335.4(LRP5):c.1827C>T (p.Asn609=) rs778446537 0.00006
NM_002335.4(LRP5):c.3337C>T (p.Arg1113Cys) rs377258285 0.00006
NM_002335.4(LRP5):c.4272C>T (p.His1424=) rs145226802 0.00006
NM_002335.4(LRP5):c.4419C>T (p.Tyr1473=) rs757191543 0.00006
NM_002335.4(LRP5):c.2827+5G>A rs373365240 0.00005
NM_002335.4(LRP5):c.4755G>A (p.Ser1585=) rs545586907 0.00005
NM_002335.4(LRP5):c.*8C>T rs758348649 0.00004
NM_002335.4(LRP5):c.171C>T (p.Ile57=) rs543962342 0.00004
NM_002335.4(LRP5):c.3843C>T (p.Asp1281=) rs200373872 0.00004
NM_002335.4(LRP5):c.3858C>T (p.Cys1286=) rs768877066 0.00004
NM_002335.4(LRP5):c.4226G>A (p.Arg1409His) rs765378705 0.00004
NM_002335.4(LRP5):c.91+9G>C rs569517144 0.00004
NM_002335.4(LRP5):c.1122C>T (p.His374=) rs764504521 0.00003
NM_002335.4(LRP5):c.228C>T (p.Ala76=) rs564857130 0.00003
NM_002335.4(LRP5):c.407A>C (p.Asn136Thr) rs759063931 0.00003
NM_002335.4(LRP5):c.4297G>A (p.Val1433Met) rs199871539 0.00003
NM_002335.4(LRP5):c.738C>T (p.Ser246=) rs768638466 0.00003
NM_002335.4(LRP5):c.1519G>A (p.Gly507Ser) rs765290711 0.00002
NM_002335.4(LRP5):c.1584+6G>C rs534512623 0.00002
NM_002335.4(LRP5):c.3198C>T (p.Arg1066=) rs370274326 0.00002
NM_002335.4(LRP5):c.1348C>T (p.Arg450Cys) rs765695793 0.00001
NM_002335.4(LRP5):c.1377C>T (p.Asp459=) rs367873767 0.00001
NM_002335.4(LRP5):c.1707G>A (p.Glu569=) rs199707305 0.00001
NM_002335.4(LRP5):c.4194C>T (p.Phe1398=) rs150618161 0.00001
NM_002335.4(LRP5):c.4488+6G>T rs751829465 0.00001
NM_002335.4(LRP5):c.920C>T (p.Ser307Phe) rs1219101402 0.00001
NM_002335.4(LRP5):c.96G>A (p.Ser32=) rs202039395 0.00001
NM_002335.4(LRP5):c.*8C>A
NM_002335.4(LRP5):c.1212G>A (p.Gly404=) rs377403217
NM_002335.4(LRP5):c.1282C>T (p.Arg428Ter) rs121908661
NM_002335.4(LRP5):c.1373T>C (p.Leu458Pro)
NM_002335.4(LRP5):c.1508G>A (p.Gly503Glu)
NM_002335.4(LRP5):c.1801+693G>A
NM_002335.4(LRP5):c.1802-8G>A
NM_002335.4(LRP5):c.1802-9C>G rs200963797
NM_002335.4(LRP5):c.204G>A (p.Val68=)
NM_002335.4(LRP5):c.2102G>A (p.Arg701His)
NM_002335.4(LRP5):c.2206G>A (p.Asp736Asn)
NM_002335.4(LRP5):c.2335G>A (p.Glu779Lys)
NM_002335.4(LRP5):c.2359G>A (p.Val787Met) rs778567335
NM_002335.4(LRP5):c.2489C>T (p.Ser830Leu)
NM_002335.4(LRP5):c.2784C>T (p.Cys928=)
NM_002335.4(LRP5):c.3070_3071del (p.Arg1024fs)
NM_002335.4(LRP5):c.3347C>T (p.Ala1116Val)
NM_002335.4(LRP5):c.3487C>T (p.Leu1163Phe) rs562616743
NM_002335.4(LRP5):c.34CTG[10] (p.Leu20dup) rs72555376
NM_002335.4(LRP5):c.375G>T (p.Thr125=) rs780348578
NM_002335.4(LRP5):c.4000+7C>G
NM_002335.4(LRP5):c.4111+3G>A
NM_002335.4(LRP5):c.4230G>A (p.Val1410=) rs752100031
NM_002335.4(LRP5):c.4434C>T (p.Val1478=)
NM_002335.4(LRP5):c.4622C>G (p.Thr1541Arg) rs150862227
NM_002335.4(LRP5):c.54_55insTTG (p.Leu20_Ala21insLeu)
NM_002335.4(LRP5):c.81C>G (p.Ala27=)
NM_002335.4(LRP5):c.92-10T>G
NM_002335.4(LRP5):c.92-7C>T

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.