rs34637584, LRRK2

N. diseases: 78
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.
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1 2006 2006
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2006 2006
Gaucher Disease
CUI: C0017205
Disease: Gaucher Disease
82 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2006 2006
Autosomal Dominant Parkinsonism
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
3 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2005 2007
Alzheimer disease, familial, type 3
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
124 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2007 2007
Tremor
CUI: C0040822
Disease: Tremor
52 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2007 2007
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
54 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2007 2008
GRN-related frontotemporal dementia
CUI: C3811918
Disease: GRN-related frontotemporal dementia
20 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2007 2008
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.030 0.667 3 2007 2009
Delusion of infidelity
CUI: C0233689
Disease: Delusion of infidelity
1 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2009 2009
Hallucinations
CUI: C0018524
Disease: Hallucinations
18 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2009 2009
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
37 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2009 2009
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2009 2009
Muscle Rigidity
CUI: C0026837
Disease: Muscle Rigidity
25 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2007 2010
Muscular stiffness
CUI: C0221170
Disease: Muscular stiffness
6 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2010 2010
Resting Tremor
CUI: C0234379
Disease: Resting Tremor
5 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2011 2011
Dementia
CUI: C0497327
Disease: Dementia
176 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 0.500 2 2006 2012
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 0.500 2 2006 2012
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2012 2013
Dopamine dysregulation syndrome
CUI: C1963757
Disease: Dopamine dysregulation syndrome
1 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2013 2013
Hallucinations, Visual
CUI: C0233763
Disease: Hallucinations, Visual
5 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2013 2013
Bradykinesia
CUI: C0233565
Disease: Bradykinesia
16 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2010 2014
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2012 2014
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2006 2014
Unspecified visual loss
CUI: C3665346
Disease: Unspecified visual loss
11 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2013 2014