rs649129, 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.
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 2 2018 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 2 2018 2019
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 2 2011 2012
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 1 2012 2012
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 1 2013 2013
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 1 2013 2013
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 1 2012 2012
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 0.700 1.000 1 2013 2013