rs1337503417, KRT16

N. diseases: 12
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.
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.050 0.600 5 2000 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.040 1.000 4 2000 2011
Obesity
CUI: C0028754
Disease: Obesity
1111 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.030 1.000 3 2006 2011
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.020 1.000 2 2003 2008
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1.000 1 2004 2004
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1.000 1 2004 2004
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1.000 1 2003 2003
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1.000 1 2004 2004
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1 2009 2009
Impaired insulin secretion
CUI: C0948379
Disease: Impaired insulin secretion
14 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1.000 1 2003 2003
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1.000 1 2001 2001
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 0.010 1.000 1 2005 2005