rs35870237, LRRK2

N. diseases: 9
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 0.763 0.120 12 40340404 missense variant T/C snv 0.800 1.000 21 2004 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.763 0.120 12 40340404 missense variant T/C snv 0.040 1.000 4 2006 2014
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
27 0.763 0.120 12 40340404 missense variant T/C snv 0.020 1.000 2 2009 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.763 0.120 12 40340404 missense variant T/C snv 0.010 1 2019 2019
Autosomal dominant late onset Parkinson disease
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
5 0.763 0.120 12 40340404 missense variant T/C snv 0.010 1.000 1 2006 2006
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.763 0.120 12 40340404 missense variant T/C snv 0.010 1.000 1 2013 2013
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.763 0.120 12 40340404 missense variant T/C snv 0.010 1.000 1 2013 2013
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.763 0.120 12 40340404 missense variant T/C snv 0.010 1.000 1 2006 2006
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.763 0.120 12 40340404 missense variant T/C snv 0.010 1.000 1 2013 2013