rs6921438, None

N. diseases: 10
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.
Vascular Endothelial Growth Factor Measurement
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
46 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.700 1.000 2 2016 2017
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.700 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.030 0.333 3 2013 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.030 1.000 3 2018 2018
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.010 1.000 1 2017 2017
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.010 1.000 1 2016 2016
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.010 1.000 1 2019 2019
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.010 1.000 1 2017 2017
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.010 1.000 1 2019 2019
Proliferative diabetic retinopathy
CUI: C0154830
Disease: Proliferative diabetic retinopathy
45 0.776 0.360 6 43957870 intergenic variant G/A;C snv 0.010 1.000 1 2019 2019