rs72551362, PPARG

N. diseases: 4
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.
Familial Partial Lipodystrophy, Type 3
CUI: C1720861
Disease: Familial Partial Lipodystrophy, Type 3
14 0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 0.700 0
Endothelial dysfunction
CUI: C0856169
Disease: Endothelial dysfunction
25 0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 0.030 1.000 3 2016 2019
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 0.010 1.000 1 2003 2003
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
28 0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 0.010 1.000 1 2005 2005