rs2276886, CXCL9

N. diseases: 3
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.
Autoimmune thyroid disease
CUI: C0178468
Disease: Autoimmune thyroid disease
15 0.882 0.120 4 76007275 intron variant C/A;T snv 0.010 1.000 1 2019 2019
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.882 0.120 4 76007275 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.882 0.120 4 76007275 intron variant C/A;T snv 0.010 1.000 1 2016 2016