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
CUI: C0020550
Disease: Hyperthyroidism
27 0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03 0.700 1.000 1 2018 2018
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03 0.700 1.000 1 2016 2016
thyroid function
CUI: C2242456
Disease: thyroid function
60 0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03 0.700 1.000 1 2010 2010