rs121909244, PPARG

N. diseases: 11
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
14 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.700 1.000 4 2000 2014
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
28 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.020 1.000 2 2005 2010
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2005 2005
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2005 2005
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2005 2005
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2010 2010
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2004 2004
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2016 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2003 2003
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2003 2003
Partial lipodystrophy
CUI: C4316789
Disease: Partial lipodystrophy
11 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2005 2005