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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.040 0.750 4 1999 2003
Congenital Hypothyroidism
CUI: C0010308
Disease: Congenital Hypothyroidism
48 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.020 1.000 2 2010 2010
Multinodular goiter
CUI: C0342208
Disease: Multinodular goiter
6 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.020 1.000 2 2013 2016
Toxic multinodular goiter
CUI: C0154143
Disease: Toxic multinodular goiter
3 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.020 1.000 2 1999 2016
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 2012 2012
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 2012 2012
Follicular thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
28 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 1999 1999
Goiter
CUI: C0018021
Disease: Goiter
19 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 2016 2016
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1 2009 2009
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
27 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1 2016 2016
Hypothyroidism, Autoimmune
CUI: C0342158
Disease: Hypothyroidism, Autoimmune
2 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 2012 2012
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 2009 2009