rs2972164, PPARG

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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.080 3 12292917 intron variant T/C snv 0.46 0.010 1 2018 2018
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.925 0.080 3 12292917 intron variant T/C snv 0.46 0.010 1.000 1 2018 2018
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.925 0.080 3 12292917 intron variant T/C snv 0.46 0.010 1.000 1 2018 2018