rs35801418, LRRK2

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
PARKINSON DISEASE 8 (disorder)
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
33 0.827 0.120 12 40321114 missense variant A/G snv 0.800 1.000 21 2004 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.827 0.120 12 40321114 missense variant A/G snv 0.030 1.000 3 2010 2018
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.827 0.120 12 40321114 missense variant A/G snv 0.010 1.000 1 2007 2007
Autosomal dominant late onset Parkinson disease
5 0.827 0.120 12 40321114 missense variant A/G snv 0.010 1.000 1 2005 2005
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.827 0.120 12 40321114 missense variant A/G snv 0.010 1.000 1 2012 2012
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.827 0.120 12 40321114 missense variant A/G snv 0.010 1.000 1 2007 2007
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.827 0.120 12 40321114 missense variant A/G snv 0.010 1.000 1 2012 2012