F11, coagulation factor XI, 2160

N. diseases: 100; N. variants: 139
Disease: Venous Thromboembolism ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2036914
rs2036914 		0.882 0.160 4 186271327 intron variant T/C snv 0.57
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.830 1.000 5 2011 2019
dbSNP: rs3756008
rs3756008 		4 186264231 upstream gene variant A/T snv 0.36
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.810 1.000 3 2011 2014
dbSNP: rs4253417
rs4253417 		4 186277851 intron variant T/C;G snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.800 1.000 3 2011 2019
dbSNP: rs4253399
rs4253399 		4 186266940 intron variant T/G snv 0.30
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.800 1.000 2 2011 2013
dbSNP: rs2289252
rs2289252 		1.000 0.040 4 186286227 non coding transcript exon variant C/T snv 0.35
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.740 1.000 5 2013 2019
dbSNP: rs925451
rs925451 		4 186266415 intron variant G/A snv 0.34
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.710 1.000 3 2010 2012
dbSNP: rs3756009
rs3756009 		4 186264957 upstream gene variant A/G snv 0.32
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 2 2011 2012
dbSNP: rs1593
rs1593 		4 186274397 3 prime UTR variant T/A;G snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4241824
rs4241824 		4 186270633 intron variant G/A snv 0.55
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4253416
rs4253416 		4 186276840 intron variant C/T snv 0.55
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4253421
rs4253421 		4 186283783 intron variant A/C;G;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2019 2019