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 0.790 0.160 14 81139828 missense variant G/A;T snv 0.700 0
Thyroid Adenoma, Hyperfunctioning
CUI: C1863960
Disease: Thyroid Adenoma, Hyperfunctioning
5 0.790 0.160 14 81139828 missense variant G/A;T snv 0.700 0
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.790 0.160 14 81139828 missense variant G/A;T snv 0.010 1.000 1 1998 1998
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.790 0.160 14 81139828 missense variant G/A;T snv 0.010 1.000 1 2008 2008
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
27 0.790 0.160 14 81139828 missense variant G/A;T snv 0.010 1.000 1 2008 2008
Secondary hyperthyroidism
CUI: C1095928
Disease: Secondary hyperthyroidism
1 0.790 0.160 14 81139828 missense variant G/A;T snv 0.010 1.000 1 2008 2008
Toxic thyroid adenoma
CUI: C0302840
Disease: Toxic thyroid adenoma
1 0.790 0.160 14 81139828 missense variant G/A;T snv 0.010 1.000 1 1997 1997