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 1, AUTOSOMAL DOMINANT (disorder)
5 0.744 0.179 4 89835580 missense variant C/G snp 0.800 6 1998 2015
Atypical Parkinson Disease
CUI: C1868596
Disease: Atypical Parkinson Disease
4 0.744 0.179 4 89835580 missense variant C/G snp 0.700 2 1998 2015
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
636 0.744 0.179 4 89835580 missense variant C/G snp 0.100 0.931 29 1999 2015
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
22 0.744 0.179 4 89835580 missense variant C/G snp 0.030 1.000 3 2001 2002
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
41 0.744 0.179 4 89835580 missense variant C/G snp 0.020 0.500 2 2002 2003
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
19 0.744 0.179 4 89835580 missense variant C/G snp 0.020 1.000 2 2000 2003
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
59 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2012 2012
Lewy Body Variant of Alzheimer Disease
3 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2000 2000
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
288 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2009 2009
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
79 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2014 2014
Motor Disorders
CUI: C0221163
Disease: Motor Disorders
3 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2004 2004
Tremor
CUI: C0040822
Disease: Tremor
27 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2004 2004
Anxiety
CUI: C0003467
Disease: Anxiety
69 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2014 2014
Linear atrophy
CUI: C0152459
Disease: Linear atrophy
3 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1 2014 2014
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
18 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2006 2006
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
87 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2009 2009
Shy-Drager Syndrome
CUI: C0037019
Disease: Shy-Drager Syndrome
27 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2003 2003