rs429699, SLC6A3

N. diseases: 3
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.
Attention deficit hyperactivity disorder
420 0.925 0.080 5 1409012 intron variant T/C snv 0.96 0.98 0.020 1.000 2 2011 2018
Inattention
CUI: C0424101
Disease: Inattention
22 0.925 0.080 5 1409012 intron variant T/C snv 0.96 0.98 0.010 1.000 1 2011 2011
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.080 5 1409012 intron variant T/C snv 0.96 0.98 0.010 1 2019 2019