rs2618431, FAM167A

N. diseases: 2
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 (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.925 0.120 8 11466955 intron variant A/G snv 0.87 0.010 1.000 1 2018 2018
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.925 0.120 8 11466955 intron variant A/G snv 0.87 0.010 1.000 1 2018 2018