ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_198578.4(LRRK2):c.356T>C (p.Leu119Pro) rs33995463 0.00140
NM_198578.4(LRRK2):c.6510C>A (p.Gly2170=) rs34869625 0.00101
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.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.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.2284C>T (p.Leu762=) rs764684819 0.00002
NM_198578.4(LRRK2):c.5948+8G>C rs756480297 0.00001
NM_198578.4(LRRK2):c.138G>C (p.Thr46=)
NM_198578.4(LRRK2):c.2370C>T (p.Leu790=)
NM_198578.4(LRRK2):c.2385C>T (p.Ala795=)
NM_198578.4(LRRK2):c.3778-355del
NM_198578.4(LRRK2):c.3778-7del
NM_198578.4(LRRK2):c.3906G>C (p.Leu1302=)
NM_198578.4(LRRK2):c.6714A>C (p.Leu2238=)
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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