ClinVar Miner

List of variants in gene LRRK2 reported as benign for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_198578.3(LRRK2):c.149A>G (p.His50Arg) rs2256408
NM_198578.3(LRRK2):c.2501-9dupT rs36220740
NM_198578.4(LRRK2):c.*364A>C rs10878441
NM_198578.4(LRRK2):c.*384C>T rs3886747
NM_198578.4(LRRK2):c.*736G>C rs1365770
NM_198578.4(LRRK2):c.*979T>C rs10784548
NM_198578.4(LRRK2):c.1102-10C>A rs7955902
NM_198578.4(LRRK2):c.1182-4A>G rs7135747
NM_198578.4(LRRK2):c.3333G>T (p.Gln1111His) rs78365431
NM_198578.4(LRRK2):c.3778-9C>T rs114948984
NM_198578.4(LRRK2):c.4541G>A (p.Arg1514Gln) rs35507033
NM_198578.4(LRRK2):c.457T>C (p.Leu153=) rs10878245
NM_198578.4(LRRK2):c.4624C>T (p.Pro1542Ser) rs33958906
NM_198578.4(LRRK2):c.4872C>A (p.Gly1624=) rs1427263
NM_198578.4(LRRK2):c.4911A>G (p.Lys1637=) rs11176013
NM_198578.4(LRRK2):c.4937T>C (p.Met1646Thr) rs35303786
NM_198578.4(LRRK2):c.5457T>C (p.Gly1819=) rs10878371
NM_198578.4(LRRK2):c.6241A>G (p.Asn2081Asp) rs33995883
NM_198578.4(LRRK2):c.7190T>C (p.Met2397Thr) rs3761863
NM_198578.4(LRRK2):c.867C>T (p.Asn289=) rs17490713

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