ClinVar Miner

List of variants reported as likely 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: 46
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HGVS dbSNP
NM_022089.4(ATP13A2):c.*243A>C rs777596557
NM_022089.4(ATP13A2):c.*251A>G rs535432261
NM_022089.4(ATP13A2):c.1005C>T (p.Ala335=) rs56290406
NM_022089.4(ATP13A2):c.1195+10G>A rs55689004
NM_022089.4(ATP13A2):c.1195+9C>T rs117758987
NM_022089.4(ATP13A2):c.1617G>T (p.Leu539=) rs61739752
NM_022089.4(ATP13A2):c.3144C>G (p.Thr1048=) rs56126202
NM_198578.4(LRRK2):c.*1181C>T rs147956597
NM_198578.4(LRRK2):c.*1446T>A rs12422278
NM_198578.4(LRRK2):c.*1464T>G rs17491828
NM_198578.4(LRRK2):c.*1482A>G rs17491835
NM_198578.4(LRRK2):c.*148T>C rs202205832
NM_198578.4(LRRK2):c.*346A>G rs17520676
NM_198578.4(LRRK2):c.*470G>T rs200678400
NM_198578.4(LRRK2):c.*936del rs367772598
NM_198578.4(LRRK2):c.*96T>C rs66737902
NM_198578.4(LRRK2):c.-124G>C rs112643657
NM_198578.4(LRRK2):c.1000G>A (p.Glu334Lys) rs78501232
NM_198578.4(LRRK2):c.1182-4A>G rs7135747
NM_198578.4(LRRK2):c.1653C>G (p.Asn551Lys) rs7308720
NM_198578.4(LRRK2):c.2167A>G (p.Ile723Val) rs10878307
NM_198578.4(LRRK2):c.2264C>T (p.Pro755Leu) rs34410987
NM_198578.4(LRRK2):c.2378G>T (p.Arg793Met) rs35173587
NM_198578.4(LRRK2):c.2689+20dup rs66810434
NM_198578.4(LRRK2):c.2857T>C (p.Leu953=) rs7966550
NM_198578.4(LRRK2):c.3333G>T (p.Gln1111His) rs78365431
NM_198578.4(LRRK2):c.3497-8del rs201739149
NM_198578.4(LRRK2):c.3778-9C>T rs114948984
NM_198578.4(LRRK2):c.4111A>G (p.Ile1371Val) rs17466213
NM_198578.4(LRRK2):c.4193G>A (p.Arg1398His) rs7133914
NM_198578.4(LRRK2):c.4229C>T (p.Thr1410Met) rs72546327
NM_198578.4(LRRK2):c.4269G>A (p.Lys1423=) rs11175964
NM_198578.4(LRRK2):c.4317+12del rs200829235
NM_198578.4(LRRK2):c.4624C>T (p.Pro1542Ser) rs33958906
NM_198578.4(LRRK2):c.4883G>C (p.Arg1628Pro) rs33949390
NM_198578.4(LRRK2):c.4937T>C (p.Met1646Thr) rs35303786
NM_198578.4(LRRK2):c.4939T>A (p.Ser1647Thr) rs11564148
NM_198578.4(LRRK2):c.5163A>G (p.Ser1721=) rs79909111
NM_198578.4(LRRK2):c.6241A>G (p.Asn2081Asp) rs33995883
NM_198578.4(LRRK2):c.6324G>A (p.Glu2108=) rs10878405
NM_198578.4(LRRK2):c.6844-14_6844-13insA rs150964683
NM_198578.4(LRRK2):c.7153G>A (p.Gly2385Arg) rs34778348
NM_198578.4(LRRK2):c.7155A>G (p.Gly2385=) rs33962975
NM_198578.4(LRRK2):c.7483G>A (p.Val2495Ile) rs150062967
NM_198578.4(LRRK2):c.867C>T (p.Asn289=) rs17490713
NM_198578.4(LRRK2):c.936G>T (p.Ala312=) rs41286466

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