rs2920502, PPARG

N. diseases: 6
Source: BEFREE ×
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.
Diabetes
CUI: C0011847
Disease: Diabetes
611 0.851 0.160 3 12287696 intron variant G/C snv 0.27 0.010 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
714 0.851 0.160 3 12287696 intron variant G/C snv 0.27 0.010 1.000 1 2018 2018
Epilepsy
CUI: C0014544
Disease: Epilepsy
250 0.851 0.160 3 12287696 intron variant G/C snv 0.27 0.010 1.000 1 2015 2015
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
59 0.851 0.160 3 12287696 intron variant G/C snv 0.27 0.010 1.000 1 2018 2018
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
80 0.851 0.160 3 12287696 intron variant G/C snv 0.27 0.010 1.000 1 2018 2018
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
189 0.851 0.160 3 12287696 intron variant G/C snv 0.27 0.010 1.000 1 2019 2019