rs653178, ATXN2

N. diseases: 17
Source: GWASDB ×
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.
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
109 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.810 1.000 2 2008 2011
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
104 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.800 1.000 1 2011 2011
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
104 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.800 1.000 1 2011 2011
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
2 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.800 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
388 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.710 1.000 1 2011 2013
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
190 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 2 2011 2011
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2272 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2013 2013
Asthma
CUI: C0004096
Disease: Asthma
263 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2011 2011
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
54 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2010 2010
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4267 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2012 2012
Diastolic blood pressure measurement
CUI: C1305849
Disease: Diastolic blood pressure measurement
30 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2009 2009
Glomerular Filtration Rate
CUI: C0017654
Disease: Glomerular Filtration Rate
14 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2013 2013
Gout
CUI: C0018099
Disease: Gout
2275 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2013 2013
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
42 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2012 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
488 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2011 2011
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
480 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2009 2009
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
14 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2013 2013