rs5443, CDCA3;GNB3

N. diseases: 106
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.
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2006 2006
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
44 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.040 0.750 4 2003 2016
Congenital contractural arachnodactyly
CUI: C0220668
Disease: Congenital contractural arachnodactyly
48 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2010 2010
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.040 0.250 4 2008 2014
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
52 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2009 2009
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1 2004 2004
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1 2014 2014
Angina Pectoris
CUI: C0002962
Disease: Angina Pectoris
65 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2006 2006
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.030 1.000 3 2002 2005
Drug-induced tardive dyskinesia
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
67 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1 2007 2007
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
67 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1 2007 2007
Hyperuricemia
CUI: C0740394
Disease: Hyperuricemia
76 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1 2006 2006
Craniosynostosis
CUI: C0010278
Disease: Craniosynostosis
90 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2019 2019
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2005 2005
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2005 2005
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2006 2006
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2014 2014
Vitelliform Macular Dystrophy
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
120 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2013 2013
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2006 2006
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2002 2002
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1 2004 2004
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.020 1.000 2 2005 2007
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2003 2003
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.040 0.750 4 1998 2000
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.020 1.000 2 2005 2018