rs7895833, None

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.
Obesity
CUI: C0028754
Disease: Obesity
1111 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.020 1.000 2 2009 2011
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.020 1.000 2 2015 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2017 2017
Craniosynostosis, Type 1
CUI: C4551902
Disease: Craniosynostosis, Type 1
28 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2019 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2012 2012
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2012 2012
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2012 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2011 2011
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2019 2019
ST segment elevation myocardial infarction
CUI: C1536220
Disease: ST segment elevation myocardial infarction
16 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.010 1.000 1 2019 2019