ClinVar Miner

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

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Total variants: 22
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HGVS dbSNP gnomAD frequency
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.3033G>T (p.Glu1011Asp) rs141252946 0.00003
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.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.2030A>C (p.His677Pro)
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.3778-4T>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.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.6844-1G>A

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