rs2393791, HNF1A

N. diseases: 8
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.
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.800 1.000 4 2013 2019
Gamma glutamyl transferase measurement
CUI: C0202035
Disease: Gamma glutamyl transferase measurement
7 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.700 1.000 1 2011 2011
Serum gamma-glutamyl transferase measurement
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
108 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.700 1.000 1 2011 2011
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.700 1.000 1 2013 2013
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.010 1.000 1 2014 2014
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.010 1.000 1 2014 2014
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.010 1.000 1 2018 2018