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.
Hyperthyroidism, Nonautoimmune
CUI: C1836706
Disease: Hyperthyroidism, Nonautoimmune
9 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.710 1.000 1 2014 2014
Congenital hyperthyroidism
CUI: C1262098
Disease: Congenital hyperthyroidism
3 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 1998 1998
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 2009 2009
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 2010 2010
Nodule
CUI: C0028259
Disease: Nodule
19 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 2005 2005
Thyrotoxicosis
CUI: C0040156
Disease: Thyrotoxicosis
7 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 1999 1999