rs628031, SLC22A1

N. diseases: 8
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.
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.020 1.000 2 2019 2019
Disruptive, Impulse Control, and Conduct Disorders
CUI: C0021122
Disease: Disruptive, Impulse Control, and Conduct Disorders
9 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.010 1.000 1 2019 2019
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.010 1.000 1 2016 2016
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.010 1.000 1 2019 2019
Hypotension, Orthostatic
CUI: C0020651
Disease: Hypotension, Orthostatic
21 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.010 1.000 1 2019 2019
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.010 1.000 1 2018 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.010 1.000 1 2019 2019
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 0.010 1.000 1 2019 2019