ClinVar Miner

List of variants reported as benign for Parkinson disease by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_022089.4(ATP13A2):c.*124C>T rs15786
NM_022089.4(ATP13A2):c.1815C>T (p.Pro605=) rs2076603
NM_022089.4(ATP13A2):c.2637C>T (p.Gly879=) rs9435662
NM_022089.4(ATP13A2):c.2790G>A (p.Ser930=) rs3738815
NM_022089.4(ATP13A2):c.2970G>A (p.Val990=) rs761421
NM_022089.4(ATP13A2):c.3084-3C>T rs7531163
NM_022089.4(ATP13A2):c.3192C>T (p.Ala1064=) rs9435659
NM_022089.4(ATP13A2):c.3516G>A (p.Pro1172=) rs3170740
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.2501-9dup rs36220740
NM_198578.4(LRRK2):c.457T>C (p.Leu153=) rs10878245
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.5457T>C (p.Gly1819=) rs10878371
NM_198578.4(LRRK2):c.7190T>C (p.Met2397Thr) rs3761863

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