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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.900 0.996 260 2005 2020
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.100 1.000 32 2006 2019
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.100 0.968 31 2005 2019
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.100 0.958 24 2005 2020
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.100 1.000 19 2005 2019
Movement Disorders
CUI: C0026650
Disease: Movement Disorders
247 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.720 1.000 10 2004 2018
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
27 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.100 1.000 10 2005 2015
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.070 0.857 7 2010 2020
PARKINSON DISEASE 8 (disorder)
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
33 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.810 1.000 7 2005 2015
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.050 1.000 5 2007 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.050 0.800 5 2010 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.050 0.800 5 2010 2020
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.040 0.750 4 2007 2019
Mitochondrial abnormalities
CUI: C4020732
Disease: Mitochondrial abnormalities
20 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.040 1.000 4 2011 2017
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
15 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.040 1.000 4 2011 2018
Sense of smell impaired
CUI: C2364082
Disease: Sense of smell impaired
12 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.040 1.000 4 2008 2018
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
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.030 1.000 3 2009 2018
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.030 1.000 3 2009 2018
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
41 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.030 0.667 3 2006 2016
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.030 1.000 3 2009 2018
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
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
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2012 2018
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.020 1.000 2 2012 2018