rs393795, SLC6A3

N. diseases: 4
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 0.160 5 1428399 intron variant G/T snv 0.28 0.030 1.000 3 2014 2019
Delirium
CUI: C0011206
Disease: Delirium
7 0.851 0.160 5 1428399 intron variant G/T snv 0.28 0.020 1.000 2 2010 2010
Attention deficit hyperactivity disorder
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
420 0.851 0.160 5 1428399 intron variant G/T snv 0.28 0.010 1.000 1 2014 2014
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.851 0.160 5 1428399 intron variant G/T snv 0.28 0.010 1.000 1 2019 2019