rs653178, ATXN2

N. diseases: 41
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.
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.810 1.000 3 2008 2011
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 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
116 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
128 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
1178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.710 1.000 2 2011 2013
Diabetes Mellitus, Insulin-Dependent
954 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.710 1.000 2 2011 2015
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 3 2009 2019
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 2 2011 2011
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 2 2015 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 2 2015 2017
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 2 2011 2016
Alopecia Areata
CUI: C0002171
Disease: Alopecia Areata
54 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2015 2015
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 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
1536 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2011 2011
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2016 2016
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2010 2010
Corpuscular Hemoglobin Concentration Mean
4389 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2012 2012
Cystatin C measurement
CUI: C1619716
Disease: Cystatin C measurement
8 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2010 2010
Diastolic blood pressure measurement
81 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2009 2009
Eczema
CUI: C0013595
Disease: Eczema
368 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2019 2019
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2016 2016
Glomerular Filtration Rate
CUI: C0017654
Disease: Glomerular Filtration Rate
1033 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
2354 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
283 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2012 2012
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2010 2010