ClinVar Miner

List of variants in gene LRRK2 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_198578.4(LRRK2):c.5163A>G (p.Ser1721=) rs79909111 0.00293
NM_198578.4(LRRK2):c.356T>C (p.Leu119Pro) rs33995463 0.00140
NM_198578.4(LRRK2):c.2378G>T (p.Arg793Met) rs35173587 0.00085
NM_198578.4(LRRK2):c.347+2T>C rs141221000 0.00084
NM_198578.4(LRRK2):c.7153G>A (p.Gly2385Arg) rs34778348 0.00058
NM_198578.4(LRRK2):c.3974G>A (p.Arg1325Gln) rs72546338 0.00021
NM_198578.4(LRRK2):c.2769G>C (p.Gln923His) rs58559150 0.00020
NM_198578.4(LRRK2):c.478T>A (p.Phe160Ile) rs746884528 0.00013
NM_198578.4(LRRK2):c.3643G>A (p.Ala1215Thr) rs143710836 0.00012
NM_198578.4(LRRK2):c.4165G>A (p.Val1389Ile) rs140743795 0.00011
NM_198578.4(LRRK2):c.2771G>A (p.Arg924His) rs200795874 0.00008
NM_198578.4(LRRK2):c.4943A>G (p.Gln1648Arg) rs200143418 0.00006
NM_198578.4(LRRK2):c.3033G>T (p.Glu1011Asp) rs141252946 0.00003
NM_198578.4(LRRK2):c.7224G>A (p.Met2408Ile) rs60545352 0.00003
NM_198578.4(LRRK2):c.7300A>G (p.Ile2434Val) rs398124661 0.00003
NM_198578.4(LRRK2):c.1132C>T (p.Leu378Phe) rs200870486 0.00002
NM_198578.4(LRRK2):c.1817G>A (p.Gly606Asp) rs138717506 0.00002
NM_198578.4(LRRK2):c.2915A>G (p.Asp972Gly) rs201718451 0.00002
NM_198578.4(LRRK2):c.2248G>A (p.Glu750Lys) rs1413463006 0.00001
NM_198578.4(LRRK2):c.3554T>C (p.Phe1185Ser) rs1358839130 0.00001
NM_198578.4(LRRK2):c.3721G>A (p.Ala1241Thr) rs767609721 0.00001
NM_198578.4(LRRK2):c.4714G>A (p.Ala1572Thr) rs1945129316 0.00001
NM_198578.4(LRRK2):c.5105T>C (p.Met1702Thr) rs200008981 0.00001
NM_198578.4(LRRK2):c.5182C>T (p.Arg1728Cys) rs201292708 0.00001
NM_198578.4(LRRK2):c.7328G>A (p.Arg2443Gln) rs774151010 0.00001
NM_198578.4(LRRK2):c.1230A>C (p.Ser410=) rs376621322
NM_198578.4(LRRK2):c.1240G>A (p.Val414Ile) rs1565682626
NM_198578.4(LRRK2):c.1250C>T (p.Ala417Val) rs1057519199
NM_198578.4(LRRK2):c.182A>G (p.His61Arg)
NM_198578.4(LRRK2):c.2030A>C (p.His677Pro)
NM_198578.4(LRRK2):c.2110A>G (p.Met704Val)
NM_198578.4(LRRK2):c.2134A>G (p.Met712Val) rs199566791
NM_198578.4(LRRK2):c.2299C>T (p.Arg767Cys)
NM_198578.4(LRRK2):c.2422T>A (p.Phe808Ile)
NM_198578.4(LRRK2):c.2428A>G (p.Ile810Val) rs72546337
NM_198578.4(LRRK2):c.267A>C (p.Ile89=) rs1364226173
NM_198578.4(LRRK2):c.2684G>A (p.Ser895Asn)
NM_198578.4(LRRK2):c.2699G>C (p.Gly900Ala) rs2136706126
NM_198578.4(LRRK2):c.3457C>T (p.Pro1153Ser)
NM_198578.4(LRRK2):c.3470G>C (p.Ser1157Thr)
NM_198578.4(LRRK2):c.352del (p.Ile118fs)
NM_198578.4(LRRK2):c.3692A>C (p.Gln1231Pro)
NM_198578.4(LRRK2):c.3778-4T>A rs1565734559
NM_198578.4(LRRK2):c.3977T>G (p.Leu1326Ter)
NM_198578.4(LRRK2):c.4128G>A (p.Trp1376Ter) rs2136815435
NM_198578.4(LRRK2):c.4289C>T (p.Ala1430Val)
NM_198578.4(LRRK2):c.4402A>G (p.Lys1468Glu) rs281865050
NM_198578.4(LRRK2):c.4417C>T (p.Leu1473Phe) rs1555187766
NM_198578.4(LRRK2):c.4433G>A (p.Gly1478Glu) rs1592270456
NM_198578.4(LRRK2):c.4540C>T (p.Arg1514Ter)
NM_198578.4(LRRK2):c.4862_4863delinsTA (p.His1621Leu) rs2136879702
NM_198578.4(LRRK2):c.4883G>A (p.Arg1628His) rs33949390
NM_198578.4(LRRK2):c.5385G>T (p.Leu1795Phe) rs111910483
NM_198578.4(LRRK2):c.5435C>T (p.Ala1812Val)
NM_198578.4(LRRK2):c.5571del (p.Asp1858fs)
NM_198578.4(LRRK2):c.5725A>T (p.Asn1909Tyr) rs2136915904
NM_198578.4(LRRK2):c.6187_6191del (p.Leu2062_Leu2063insTer) rs111739194
NM_198578.4(LRRK2):c.6317T>C (p.Met2106Thr)
NM_198578.4(LRRK2):c.6466G>T (p.Val2156Phe) rs1555194625
NM_198578.4(LRRK2):c.6770G>A (p.Ser2257Asn)
NM_198578.4(LRRK2):c.6844-1G>A
NM_198578.4(LRRK2):c.6903G>A (p.Met2301Ile)
NM_198578.4(LRRK2):c.7348A>G (p.Asn2450Asp)
NM_198578.4(LRRK2):c.7374G>C (p.Met2458Ile) rs765994542
NM_198578.4(LRRK2):c.7450C>A (p.Gln2484Lys)
NM_198578.4(LRRK2):c.7510G>C (p.Val2504Leu) rs1946922213
NM_198578.4(LRRK2):c.751A>G (p.Asn251Asp)

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