rs188286943, VPS35

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 17
CUI: C3280133
Disease: PARKINSON DISEASE 17
1 0.776 0.160 16 46662452 missense variant C/T snv 0.700 0
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.776 0.160 16 46662452 missense variant C/T snv 0.100 0.957 23 2012 2019
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
27 0.776 0.160 16 46662452 missense variant C/T snv 0.060 1.000 6 2012 2014
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.776 0.160 16 46662452 missense variant C/T snv 0.040 1.000 4 2011 2015
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.776 0.160 16 46662452 missense variant C/T snv 0.040 1.000 4 2011 2015
Autosomal dominant late onset Parkinson disease
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
5 0.776 0.160 16 46662452 missense variant C/T snv 0.020 1.000 2 2011 2017
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.776 0.160 16 46662452 missense variant C/T snv 0.020 0.500 2 2013 2014
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.776 0.160 16 46662452 missense variant C/T snv 0.010 1.000 1 2015 2015
Wiskott-Aldrich Syndrome
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
34 0.776 0.160 16 46662452 missense variant C/T snv 0.010 1.000 1 2014 2014