rs121909244, PPARG

N. diseases: 10
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.
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
26 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
611 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
714 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
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
1598 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
79 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
871 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
80 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
477 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
15 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