rs225014, DIO2

N. diseases: 22
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.
Thyroxine measurement
CUI: C0202231
Disease: Thyroxine measurement
42 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.700 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.060 0.833 6 2005 2016
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.050 1.000 5 2013 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.030 1.000 3 2004 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.030 0.667 3 2007 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.020 1.000 2 2007 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.020 0.500 2 2007 2018
Kashin-Beck Disease
CUI: C2745963
Disease: Kashin-Beck Disease
43 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.020 2 2013 2016
Obesity
CUI: C0028754
Disease: Obesity
1111 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.020 2 2007 2012
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2013 2013
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2009 2009
Degenerative disorder
CUI: C1285162
Disease: Degenerative disorder
6 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2018 2018
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2012 2012
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2010 2010
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2018 2018
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2010 2010
Osteoarthritis of hip
CUI: C0029410
Disease: Osteoarthritis of hip
121 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2008 2008
Recurrent depression
CUI: C0221480
Disease: Recurrent depression
12 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2015 2015
Recurrent depressive disorder
CUI: C0349218
Disease: Recurrent depressive disorder
9 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2015 2015
Severe Sepsis
CUI: C1719672
Disease: Severe Sepsis
29 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2011 2011
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2018 2018
Thyroid Hormone Metabolism, Abnormal
CUI: C1864761
Disease: Thyroid Hormone Metabolism, Abnormal
5 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2018 2018