ClinVar Miner

List of variants in gene LRP5 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 121
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002335.4(LRP5):c.1801+675A>G rs555106014 0.00188
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.1032G>C (p.Leu344=) rs143499301 0.00048
NM_002335.4(LRP5):c.4256A>G (p.Asn1419Ser) rs145750689 0.00046
NM_002335.4(LRP5):c.2829G>A (p.Pro943=) rs201018263 0.00044
NM_002335.4(LRP5):c.2324T>C (p.Ile775Thr) rs144983823 0.00042
NM_002335.4(LRP5):c.2182A>T (p.Met728Leu) rs149241739 0.00038
NM_002335.4(LRP5):c.4511C>T (p.Pro1504Leu) rs201475647 0.00038
NM_002335.4(LRP5):c.3403C>T (p.Arg1135Cys) rs143396225 0.00031
NM_002335.4(LRP5):c.4565C>T (p.Pro1522Leu) rs200624778 0.00026
NM_002335.4(LRP5):c.1738G>A (p.Val580Ile) rs149524398 0.00024
NM_002335.4(LRP5):c.1199C>T (p.Ala400Val) rs201320326 0.00014
NM_002335.4(LRP5):c.3901G>A (p.Ala1301Thr) rs149166384 0.00013
NM_002335.4(LRP5):c.164C>T (p.Ser55Phe) rs148462220 0.00011
NM_002335.4(LRP5):c.3245A>G (p.Tyr1082Cys) rs113804402 0.00010
NM_002335.4(LRP5):c.3586G>A (p.Ala1196Thr) rs199887400 0.00010
NM_002335.4(LRP5):c.4643G>T (p.Cys1548Phe) rs147618989 0.00010
NM_002335.4(LRP5):c.1744A>G (p.Ile582Val) rs1056743758 0.00009
NM_002335.4(LRP5):c.3028C>T (p.Pro1010Ser) rs201793593 0.00009
NM_002335.4(LRP5):c.2363G>A (p.Arg788Gln) rs771972596 0.00008
NM_002335.4(LRP5):c.2951A>G (p.Tyr984Cys) rs759674127 0.00006
NM_002335.4(LRP5):c.3337C>T (p.Arg1113Cys) rs377258285 0.00006
NM_002335.4(LRP5):c.3553G>A (p.Gly1185Arg) rs375557997 0.00005
NM_002335.4(LRP5):c.4610C>T (p.Ala1537Val) rs753256748 0.00005
NM_002335.4(LRP5):c.4791G>C (p.Glu1597Asp) rs142508112 0.00005
NM_002335.4(LRP5):c.1226C>T (p.Thr409Met) rs199686378 0.00004
NM_002335.4(LRP5):c.3266G>A (p.Arg1089Gln) rs373906355 0.00004
NM_002335.4(LRP5):c.4142C>T (p.Pro1381Leu) rs369637767 0.00004
NM_002335.4(LRP5):c.1613G>A (p.Arg538Gln) rs138692892 0.00003
NM_002335.4(LRP5):c.3581G>A (p.Arg1194His) rs201017887 0.00003
NM_002335.4(LRP5):c.4268C>T (p.Pro1423Leu) rs748143518 0.00003
NM_002335.4(LRP5):c.1220C>T (p.Ala407Val) rs369125661 0.00002
NM_002335.4(LRP5):c.3307C>T (p.Arg1103Cys) rs768840999 0.00002
NM_002335.4(LRP5):c.796C>T (p.Arg266Cys) rs368484557 0.00002
NM_002335.4(LRP5):c.1182G>A (p.Val394=) rs746800397 0.00001
NM_002335.4(LRP5):c.1183C>T (p.Arg395Trp) rs1177481438 0.00001
NM_002335.4(LRP5):c.119G>A (p.Arg40His) rs2098614505 0.00001
NM_002335.4(LRP5):c.1300G>A (p.Asp434Asn) rs757888034 0.00001
NM_002335.4(LRP5):c.1315C>T (p.Arg439Cys) rs1218658711 0.00001
NM_002335.4(LRP5):c.1316G>A (p.Arg439His) rs201547952 0.00001
NM_002335.4(LRP5):c.1385G>A (p.Arg462Gln) rs756952499 0.00001
NM_002335.4(LRP5):c.1440G>T (p.Glu480Asp) rs2496621838 0.00001
NM_002335.4(LRP5):c.1571C>G (p.Thr524Arg) rs2098645456 0.00001
NM_002335.4(LRP5):c.1910T>C (p.Met637Thr) rs1045994595 0.00001
NM_002335.4(LRP5):c.1960G>A (p.Ala654Thr) rs747131775 0.00001
NM_002335.4(LRP5):c.2092A>G (p.Thr698Ala) rs1196921878 0.00001
NM_002335.4(LRP5):c.213G>C (p.Gln71His) rs1242896791 0.00001
NM_002335.4(LRP5):c.2241G>A (p.Leu747=) rs867927445 0.00001
NM_002335.4(LRP5):c.2254C>T (p.Arg752Trp) rs121908674 0.00001
NM_002335.4(LRP5):c.283A>C (p.Thr95Pro) rs771960523 0.00001
NM_002335.4(LRP5):c.3280G>A (p.Glu1094Lys) rs1433868957 0.00001
NM_002335.4(LRP5):c.3392C>T (p.Ala1131Val) rs199960554 0.00001
NM_002335.4(LRP5):c.3443C>T (p.Thr1148Ile) rs771190332 0.00001
NM_002335.4(LRP5):c.3515G>A (p.Arg1172His) rs751672886 0.00001
NM_002335.4(LRP5):c.3568C>T (p.Arg1190Cys) rs767540992 0.00001
NM_002335.4(LRP5):c.3763+2T>C rs774270653 0.00001
NM_002335.4(LRP5):c.4200G>C (p.Met1400Ile) rs748007622 0.00001
NM_002335.4(LRP5):c.4258G>A (p.Gly1420Arg) rs778832210 0.00001
NM_002335.4(LRP5):c.4273G>A (p.Glu1425Lys) rs1339305831 0.00001
NM_002335.4(LRP5):c.4337G>T (p.Gly1446Val) rs143166423 0.00001
NM_002335.4(LRP5):c.4487C>T (p.Pro1496Leu) rs778202459 0.00001
NM_002335.4(LRP5):c.4502C>T (p.Pro1501Leu) rs867899944 0.00001
NM_002335.4(LRP5):c.4666C>T (p.Arg1556Cys) rs140474222 0.00001
NM_002335.4(LRP5):c.754T>G (p.Trp252Gly) rs765637520 0.00001
NM_002335.4(LRP5):c.98C>T (p.Pro33Leu) rs753259758 0.00001
NM_002335.4(LRP5):c.1007G>A (p.Cys336Tyr) rs139896674
NM_002335.4(LRP5):c.1027G>A (p.Val343Met) rs761479086
NM_002335.4(LRP5):c.1043G>A (p.Arg348Gln)
NM_002335.4(LRP5):c.1133T>A (p.Ile378Asn) rs2496598111
NM_002335.4(LRP5):c.1141G>A (p.Asp381Asn) rs1332274863
NM_002335.4(LRP5):c.1172A>T (p.Asp391Val) rs1323247011
NM_002335.4(LRP5):c.1256A>G (p.Asp419Gly) rs2496599301
NM_002335.4(LRP5):c.1328C>A (p.Thr443Lys) rs200416179
NM_002335.4(LRP5):c.1514C>T (p.Pro505Leu)
NM_002335.4(LRP5):c.1678T>C (p.Trp560Arg) rs1192536581
NM_002335.4(LRP5):c.1736A>G (p.Asp579Gly) rs2153163058
NM_002335.4(LRP5):c.1748A>T (p.Asp583Val) rs1064796661
NM_002335.4(LRP5):c.1793A>G (p.Lys598Arg) rs1161765642
NM_002335.4(LRP5):c.1828G>A (p.Gly610Arg) rs80358313
NM_002335.4(LRP5):c.1912A>G (p.Lys638Glu) rs758976409
NM_002335.4(LRP5):c.2208C>A (p.Asp736Glu) rs35298380
NM_002335.4(LRP5):c.2312C>T (p.Thr771Ile)
NM_002335.4(LRP5):c.2318G>A (p.Gly773Asp) rs2098658610
NM_002335.4(LRP5):c.2378G>T (p.Gly793Val) rs2153167061
NM_002335.4(LRP5):c.2384A>G (p.Asn795Ser) rs368485424
NM_002335.4(LRP5):c.2386T>C (p.Cys796Arg) rs1487357243
NM_002335.4(LRP5):c.2432T>C (p.Ile811Thr) rs1261083418
NM_002335.4(LRP5):c.2513G>A (p.Arg838Gln) rs559129140
NM_002335.4(LRP5):c.2564G>A (p.Ser855Asn) rs2153168056
NM_002335.4(LRP5):c.2721G>A (p.Met907Ile) rs757489082
NM_002335.4(LRP5):c.2740G>A (p.Gly914Arg) rs2098661042
NM_002335.4(LRP5):c.2972T>C (p.Ile991Thr) rs1565094883
NM_002335.4(LRP5):c.317G>T (p.Gly106Val) rs1442757499
NM_002335.4(LRP5):c.3277A>T (p.Ile1093Phe) rs780548194
NM_002335.4(LRP5):c.3308G>T (p.Arg1103Leu) rs566582167
NM_002335.4(LRP5):c.3326C>A (p.Thr1109Asn) rs2153173911
NM_002335.4(LRP5):c.3404G>A (p.Arg1135His) rs560826688
NM_002335.4(LRP5):c.3422T>G (p.Leu1141Arg) rs1457319820
NM_002335.4(LRP5):c.3446T>A (p.Leu1149Gln) rs200389686
NM_002335.4(LRP5):c.346G>A (p.Asp116Asn)
NM_002335.4(LRP5):c.34CTG[11] (p.Leu19_Leu20dup) rs72555376
NM_002335.4(LRP5):c.34CTG[12] (p.Leu18_Leu20dup) rs72555376
NM_002335.4(LRP5):c.34CTG[15] (p.Leu15_Leu20dup) rs72555376
NM_002335.4(LRP5):c.3592C>T (p.Leu1198Phe) rs1287001576
NM_002335.4(LRP5):c.3764-3C>A rs200397490
NM_002335.4(LRP5):c.3796T>C (p.Cys1266Arg)
NM_002335.4(LRP5):c.3934G>A (p.Asp1312Asn)
NM_002335.4(LRP5):c.4027T>C (p.Cys1343Arg) rs1171090375
NM_002335.4(LRP5):c.4201G>A (p.Gly1401Ser)
NM_002335.4(LRP5):c.425G>C (p.Arg142Pro) rs368198391
NM_002335.4(LRP5):c.4352T>G (p.Ile1451Ser) rs1176509894
NM_002335.4(LRP5):c.4388T>C (p.Leu1463Pro) rs2496908011
NM_002335.4(LRP5):c.4535A>G (p.Asn1512Ser)
NM_002335.4(LRP5):c.4778C>T (p.Ser1593Leu) rs1205746483
NM_002335.4(LRP5):c.494T>C (p.Met165Thr) rs1023373570
NM_002335.4(LRP5):c.495G>T (p.Met165Ile)
NM_002335.4(LRP5):c.533G>T (p.Arg178Leu) rs183377804
NM_002335.4(LRP5):c.580A>G (p.Ile194Val) rs2098624345
NM_002335.4(LRP5):c.58_69dup (p.Leu20_Cys23dup) rs2153110216
NM_002335.4(LRP5):c.701_703del (p.Glu234del)

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.