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 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.900 1.000 16 2009 2020
Chronic constipation
CUI: C0401149
Disease: Chronic constipation
16 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.010 1.000 1 2015 2015
Dementia
CUI: C0497327
Disease: Dementia
176 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
15 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
Sense of smell impaired
CUI: C2364082
Disease: Sense of smell impaired
12 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.010 1.000 1 2015 2015
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.010 1.000 1 2017 2017