ClinVar Miner

List of variants reported for Autosomal dominant Parkinson disease 8 by Fulgent Genetics, Fulgent Genetics

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_198578.4(LRRK2):c.4939T>A (p.Ser1647Thr) rs11564148 0.26687
NM_198578.4(LRRK2):c.6324G>A (p.Glu2108=) rs10878405 0.26650
NM_198578.4(LRRK2):c.7155A>G (p.Gly2385=) rs33962975 0.11278
NM_198578.4(LRRK2):c.1653C>G (p.Asn551Lys) rs7308720 0.10004
NM_198578.4(LRRK2):c.2857T>C (p.Leu953=) rs7966550 0.08994
NM_198578.4(LRRK2):c.4269G>A (p.Lys1423=) rs11175964 0.05959
NM_198578.4(LRRK2):c.4624C>T (p.Pro1542Ser) rs33958906 0.03091
NM_198578.4(LRRK2):c.6844-14_6844-13insA rs150964683 0.01681
NM_198578.4(LRRK2):c.3778-9C>T rs114948984 0.01375
NM_198578.4(LRRK2):c.5509+20A>C rs11564134 0.01309
NM_198578.4(LRRK2):c.6241A>G (p.Asn2081Asp) rs33995883 0.01276
NM_198578.4(LRRK2):c.867C>T (p.Asn289=) rs17490713 0.01182
NM_198578.4(LRRK2):c.3784C>G (p.Pro1262Ala) rs4640000 0.00717
NM_198578.4(LRRK2):c.4541G>A (p.Arg1514Gln) rs35507033 0.00526
NM_198578.4(LRRK2):c.5510-9A>G rs41286460 0.00252
NM_198578.4(LRRK2):c.3333G>T (p.Gln1111His) rs78365431 0.00121
NM_198578.4(LRRK2):c.6566A>G (p.Tyr2189Cys) rs35658131 0.00055
NM_198578.4(LRRK2):c.1383T>C (p.Ser461=) rs35847451 0.00047
NM_198578.4(LRRK2):c.2481T>C (p.Ser827=) rs76890302 0.00038
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.1256C>T (p.Ala419Val) rs34594498 0.00025
NM_198578.4(LRRK2):c.7462+15G>C rs200420425 0.00025
NM_198578.4(LRRK2):c.2264C>T (p.Pro755Leu) rs34410987 0.00023
NM_198578.4(LRRK2):c.1324C>T (p.His442Tyr) rs568593066 0.00022
NM_198578.4(LRRK2):c.5822G>A (p.Arg1941His) rs77428810 0.00022
NM_198578.4(LRRK2):c.45T>C (p.Thr15=) rs142399623 0.00019
NM_198578.4(LRRK2):c.3643G>A (p.Ala1215Thr) rs143710836 0.00012
NM_198578.4(LRRK2):c.2229T>G (p.Ser743=) rs200425243 0.00011
NM_198578.4(LRRK2):c.2771G>A (p.Arg924His) rs200795874 0.00008
NM_198578.4(LRRK2):c.309G>C (p.Gln103His) rs200926937 0.00008
NM_198578.4(LRRK2):c.683G>C (p.Cys228Ser) rs56108242 0.00008
NM_198578.4(LRRK2):c.546A>G (p.Lys182=) rs35517158 0.00006
NM_198578.4(LRRK2):c.6928A>G (p.Thr2310Ala) rs202179802 0.00006
NM_198578.4(LRRK2):c.1874A>G (p.His625Arg) rs200787476 0.00005
NM_198578.4(LRRK2):c.1546A>G (p.Met516Val) rs746747483 0.00004
NM_198578.4(LRRK2):c.2758G>A (p.Ala920Thr) rs201184634 0.00004
NM_198578.4(LRRK2):c.3018A>G (p.Ile1006Met) rs113217062 0.00004
NM_198578.4(LRRK2):c.3595C>T (p.Arg1199Trp) rs746433333 0.00004
NM_198578.4(LRRK2):c.137C>T (p.Thr46Met) rs781394575 0.00003
NM_198578.4(LRRK2):c.1987T>C (p.Ser663Pro) rs78154388 0.00003
NM_198578.4(LRRK2):c.3091T>C (p.Cys1031Arg) rs201552816 0.00003
NM_198578.4(LRRK2):c.4321C>T (p.Arg1441Cys) rs33939927 0.00003
NM_198578.4(LRRK2):c.5870G>T (p.Arg1957Leu) rs201012950 0.00003
NM_198578.4(LRRK2):c.5931C>T (p.His1977=) rs201119482 0.00003
NM_198578.4(LRRK2):c.7382C>T (p.Ala2461Val) rs201037550 0.00003
NM_198578.4(LRRK2):c.7186_7187dup (p.Val2396_Met2397insTer) rs281865056 0.00002
NM_198578.4(LRRK2):c.2333G>A (p.Ser778Asn) rs1356461363 0.00001
NM_198578.4(LRRK2):c.4117G>A (p.Val1373Met) rs756381499 0.00001
NM_198578.4(LRRK2):c.500T>G (p.Met167Arg) rs201411683 0.00001
NM_198578.4(LRRK2):c.6220G>A (p.Val2074Ile) rs200498558 0.00001
NM_198578.4(LRRK2):c.7324C>T (p.Arg2442Cys) rs199893519 0.00001
NM_198578.4(LRRK2):c.1240G>A (p.Val414Ile) rs1565682626
NM_198578.4(LRRK2):c.2689+19_2689+20dup rs66810434
NM_198578.4(LRRK2):c.2689+20dup rs66810434
NM_198578.4(LRRK2):c.3497-8del rs201739149
NM_198578.4(LRRK2):c.4193G>A (p.Arg1398His) rs7133914
NM_198578.4(LRRK2):c.5183G>T (p.Arg1728Leu) rs145364431
NM_198578.4(LRRK2):c.6187_6191del (p.Leu2062_Leu2063insTer) rs111739194
NM_198578.4(LRRK2):c.6844-8dup rs72546334
NM_198578.4(LRRK2):c.7146A>C (p.Lys2382Asn) rs919570241
NM_198578.4(LRRK2):c.7430G>A (p.Arg2477Gln) rs146428335
NM_198578.4(LRRK2):c.936G>T (p.Ala312=) rs41286466

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