rs2069849, IL6

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.
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02 0.010 1.000 1 2019 2019
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02 0.010 1.000 1 2019 2019
Selective immunoglobulin A deficiency
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
23 0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02 0.010 1.000 1 2008 2008