rs2036914, F11

N. diseases: 5
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.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.830 1.000 5 2011 2019
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.020 1.000 2 2009 2016
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.010 1.000 1 2019 2019
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.010 1.000 1 2019 2019