ClinVar Miner

List of variants in gene LRRK2 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_198578.4(LRRK2):c.4541G>A (p.Arg1514Gln) rs35507033 0.00526
NM_198578.4(LRRK2):c.4318-6C>T rs56082834 0.00339
NM_198578.4(LRRK2):c.1000G>A (p.Glu334Lys) rs78501232 0.00266
NM_198578.4(LRRK2):c.*123A>C rs73277568 0.00159
NM_198578.4(LRRK2):c.356T>C (p.Leu119Pro) rs33995463 0.00140
NM_198578.4(LRRK2):c.*1402G>T rs201559861 0.00107
NM_198578.4(LRRK2):c.6510C>A (p.Gly2170=) rs34869625 0.00101
NM_198578.4(LRRK2):c.3777+7C>T rs41286480 0.00097
NM_198578.4(LRRK2):c.5606T>C (p.Met1869Thr) rs35602796 0.00060
NM_198578.4(LRRK2):c.4111A>G (p.Ile1371Val) rs17466213 0.00050
NM_198578.4(LRRK2):c.1383T>C (p.Ser461=) rs35847451 0.00047
NM_198578.4(LRRK2):c.825T>C (p.His275=) rs72546315 0.00041
NM_198578.4(LRRK2):c.6055G>A (p.Gly2019Ser) rs34637584 0.00036
NM_198578.4(LRRK2):c.7429C>T (p.Arg2477Trp) rs138780308 0.00035
NM_198578.4(LRRK2):c.364C>T (p.Leu122=) rs41286468 0.00026
NM_198578.4(LRRK2):c.1256C>T (p.Ala419Val) rs34594498 0.00025
NM_198578.4(LRRK2):c.7067C>T (p.Thr2356Ile) rs113511708 0.00025
NM_198578.4(LRRK2):c.6801C>T (p.Thr2267=) rs148143226 0.00023
NM_198578.4(LRRK2):c.5799A>T (p.Ile1933=) rs139746572 0.00021
NM_198578.4(LRRK2):c.2769G>C (p.Gln923His) rs58559150 0.00020
NM_198578.4(LRRK2):c.3429C>T (p.Ser1143=) rs142989436 0.00019
NM_198578.4(LRRK2):c.3683G>C (p.Ser1228Thr) rs60185966 0.00019
NM_198578.4(LRRK2):c.3342A>G (p.Leu1114=) rs35808389 0.00016
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.632C>T (p.Ala211Val) rs112794616 0.00011
NM_198578.4(LRRK2):c.7483G>A (p.Val2495Ile) rs150062967 0.00011
NM_198578.4(LRRK2):c.3960G>T (p.Arg1320Ser) rs77018758 0.00009
NM_198578.4(LRRK2):c.2771G>A (p.Arg924His) rs200795874 0.00008
NM_198578.4(LRRK2):c.6928A>G (p.Thr2310Ala) rs202179802 0.00006
NM_198578.4(LRRK2):c.4881G>A (p.Ser1627=) rs767307387 0.00005
NM_198578.4(LRRK2):c.6422C>T (p.Thr2141Met) rs111691891 0.00005
NM_198578.4(LRRK2):c.2758G>A (p.Ala920Thr) rs201184634 0.00004
NM_198578.4(LRRK2):c.3846A>T (p.Arg1282Ser) rs886344692 0.00004
NM_198578.4(LRRK2):c.3993T>G (p.Pro1331=) rs141293633 0.00004
NM_198578.4(LRRK2):c.6929C>T (p.Thr2310Met) rs200002022 0.00004
NM_198578.4(LRRK2):c.1446A>G (p.Ala482=) rs757454147 0.00003
NM_198578.4(LRRK2):c.3033G>T (p.Glu1011Asp) rs141252946 0.00003
NM_198578.4(LRRK2):c.4321C>T (p.Arg1441Cys) rs33939927 0.00003
NM_198578.4(LRRK2):c.2284C>T (p.Leu762=) rs764684819 0.00002
NM_198578.4(LRRK2):c.2248G>A (p.Glu750Lys) rs1413463006 0.00001
NM_198578.4(LRRK2):c.5105T>C (p.Met1702Thr) rs200008981 0.00001
NM_198578.4(LRRK2):c.5948+8G>C rs756480297 0.00001
NM_198578.4(LRRK2):c.7328G>A (p.Arg2443Gln) rs774151010 0.00001
NM_198578.4(LRRK2):c.*131del rs572544182
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.138G>C (p.Thr46=)
NM_198578.4(LRRK2):c.2030A>C (p.His677Pro)
NM_198578.4(LRRK2):c.2370C>T (p.Leu790=)
NM_198578.4(LRRK2):c.2385C>T (p.Ala795=)
NM_198578.4(LRRK2):c.267A>C (p.Ile89=) rs1364226173
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.3778-355del
NM_198578.4(LRRK2):c.3778-4T>A rs1565734559
NM_198578.4(LRRK2):c.3778-7del
NM_198578.4(LRRK2):c.3906G>C (p.Leu1302=)
NM_198578.4(LRRK2):c.3977T>G (p.Leu1326Ter)
NM_198578.4(LRRK2):c.4128G>A (p.Trp1376Ter) rs2136815435
NM_198578.4(LRRK2):c.4310A>G (p.Asn1437Ser) rs1944946235
NM_198578.4(LRRK2):c.4433G>A (p.Gly1478Glu) rs1592270456
NM_198578.4(LRRK2):c.4540C>T (p.Arg1514Ter)
NM_198578.4(LRRK2):c.4883G>A (p.Arg1628His) rs33949390
NM_198578.4(LRRK2):c.5435C>T (p.Ala1812Val)
NM_198578.4(LRRK2):c.6059T>C (p.Ile2020Thr) rs35870237
NM_198578.4(LRRK2):c.6714A>C (p.Leu2238=)
NM_198578.4(LRRK2):c.6844-1G>A
NM_198578.4(LRRK2):c.7074G>T (p.Val2358=)
NM_198578.4(LRRK2):c.7337G>A (p.Arg2446His)
NM_198578.4(LRRK2):c.936G>T (p.Ala312=) rs41286466

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