ClinVar Miner

List of variants in gene LRP5 reported by Ambry Genetics

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Gene type:
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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_002335.4(LRP5):c.1199C>T (p.Ala400Val) rs201320326 0.00014
NM_002335.4(LRP5):c.3793G>C (p.Ala1265Pro) rs201530801 0.00014
NM_002335.4(LRP5):c.3279C>G (p.Ile1093Met) rs140852936 0.00013
NM_002335.4(LRP5):c.1798G>A (p.Val600Ile) rs143878170 0.00009
NM_002335.4(LRP5):c.1132A>G (p.Ile378Val) rs369747444 0.00008
NM_002335.4(LRP5):c.4016A>G (p.Asn1339Ser) rs142001526 0.00008
NM_002335.4(LRP5):c.1283G>A (p.Arg428Gln) rs770223547 0.00007
NM_002335.4(LRP5):c.1636C>T (p.Pro546Ser) rs774097621 0.00006
NM_002335.4(LRP5):c.2951A>G (p.Tyr984Cys) rs759674127 0.00006
NM_002335.4(LRP5):c.3199G>A (p.Asp1067Asn) rs747518922 0.00006
NM_002335.4(LRP5):c.2393C>T (p.Thr798Met) rs371155552 0.00005
NM_002335.4(LRP5):c.680C>T (p.Ser227Leu) rs200384949 0.00005
NM_002335.4(LRP5):c.2518G>A (p.Val840Met) rs757262154 0.00004
NM_002335.4(LRP5):c.3196C>T (p.Arg1066Cys) rs201285828 0.00004
NM_002335.4(LRP5):c.4292C>T (p.Pro1431Leu) rs561503730 0.00004
NM_002335.4(LRP5):c.3829G>T (p.Ala1277Ser) rs754686025 0.00003
NM_002335.4(LRP5):c.148G>A (p.Gly50Arg) rs558895370 0.00002
NM_002335.4(LRP5):c.2057A>G (p.Asn686Ser) rs746188108 0.00002
NM_002335.4(LRP5):c.4225C>T (p.Arg1409Cys) rs759834541 0.00002
NM_002335.4(LRP5):c.1310C>T (p.Thr437Met) rs370901051 0.00001
NM_002335.4(LRP5):c.1528C>G (p.Leu510Val) rs752625747 0.00001
NM_002335.4(LRP5):c.1709G>A (p.Arg570Gln) rs80358312 0.00001
NM_002335.4(LRP5):c.1948A>G (p.Thr650Ala) rs756999448 0.00001
NM_002335.4(LRP5):c.2548G>A (p.Gly850Ser) rs776947784 0.00001
NM_002335.4(LRP5):c.3148G>A (p.Val1050Ile) rs577519439 0.00001
NM_002335.4(LRP5):c.4036G>A (p.Gly1346Ser) rs747638441 0.00001
NM_002335.4(LRP5):c.913G>A (p.Gly305Ser) rs377176311 0.00001
NM_002335.4(LRP5):c.1015G>A (p.Gly339Arg)
NM_002335.4(LRP5):c.140A>G (p.Asp47Gly)
NM_002335.4(LRP5):c.1993A>C (p.Asn665His)
NM_002335.4(LRP5):c.2111T>C (p.Met704Thr) rs2098658465
NM_002335.4(LRP5):c.2284A>G (p.Asn762Asp)
NM_002335.4(LRP5):c.2365G>A (p.Ala789Thr)
NM_002335.4(LRP5):c.2389A>G (p.Met797Val)
NM_002335.4(LRP5):c.2499G>A (p.Met833Ile)
NM_002335.4(LRP5):c.2630G>A (p.Arg877Gln)
NM_002335.4(LRP5):c.2718_2721del (p.Met907fs) rs1244761864
NM_002335.4(LRP5):c.2779G>A (p.Gly927Ser) rs764138752
NM_002335.4(LRP5):c.2828C>T (p.Pro943Leu)
NM_002335.4(LRP5):c.3101A>G (p.Tyr1034Cys)
NM_002335.4(LRP5):c.3136A>G (p.Asn1046Asp)
NM_002335.4(LRP5):c.3232C>T (p.Arg1078Ter) rs765402802
NM_002335.4(LRP5):c.3353T>C (p.Val1118Ala)
NM_002335.4(LRP5):c.3476G>A (p.Gly1159Asp)
NM_002335.4(LRP5):c.34CTG[11] (p.Leu19_Leu20dup) rs72555376
NM_002335.4(LRP5):c.3568C>T (p.Arg1190Cys)
NM_002335.4(LRP5):c.3641C>T (p.Ala1214Val)
NM_002335.4(LRP5):c.4228G>A (p.Val1410Met)
NM_002335.4(LRP5):c.4408G>A (p.Val1470Met)
NM_002335.4(LRP5):c.4454_4465del (p.Ser1485_Ser1488del) rs774251511
NM_002335.4(LRP5):c.4488+2T>G rs80358322
NM_002335.4(LRP5):c.4622C>G (p.Thr1541Arg) rs150862227
NM_002335.4(LRP5):c.4636G>A (p.Asp1546Asn)
NM_002335.4(LRP5):c.4669T>G (p.Trp1557Gly)
NM_002335.4(LRP5):c.500G>C (p.Trp167Ser) rs770383372
NM_002335.4(LRP5):c.71G>A (p.Gly24Asp)
NM_002335.4(LRP5):c.908A>G (p.Asn303Ser)
NM_002335.4(LRP5):c.934C>G (p.Leu312Val)
NM_002335.4(LRP5):c.998G>A (p.Gly333Asp) rs764782174

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