rs40184, SLC6A3

N. diseases: 5
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.
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.851 0.120 5 1394962 intron variant C/T snv 0.45 0.020 1.000 2 2008 2010
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.851 0.120 5 1394962 intron variant C/T snv 0.45 0.020 1.000 2 2008 2010
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.851 0.120 5 1394962 intron variant C/T snv 0.45 0.010 1.000 1 2015 2015
Hyperprolactinemia
CUI: C0020514
Disease: Hyperprolactinemia
10 0.851 0.120 5 1394962 intron variant C/T snv 0.45 0.010 1.000 1 2019 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.120 5 1394962 intron variant C/T snv 0.45 0.010 1.000 1 2019 2019