rs2273773, SIRT1

N. diseases: 9
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.020 1.000 2 2011 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2014 2014
Craniosynostosis, Type 1
CUI: C4551902
Disease: Craniosynostosis, Type 1
28 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2019 2019
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2015 2015
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2012 2012
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2012 2012
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2011 2011
Obesity
CUI: C0028754
Disease: Obesity
1111 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2011 2011
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2015 2015