rs6679356, IL12RB2

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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.925 0.200 1 67354511 intron variant C/T snv 0.75 0.700 1.000 1 2015 2015
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.925 0.200 1 67354511 intron variant C/T snv 0.75 0.010 1.000 1 2018 2018