Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2289252
rs2289252
F11 ; F11-AS1
1.000 0.040 4 186286227 non coding transcript exon variant C/T snv 0.35
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.740 1.000 5 2013 2019
dbSNP: rs10025152
rs10025152
F11-AS1
4 186304150 intron variant G/A snv 0.20
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs10029715
rs10029715
F11-AS1
4 186301446 intron variant T/C snv 0.22
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs1008728
rs1008728
F11-AS1
4 186305519 intron variant C/T snv 0.57
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs11132387
rs11132387
F11-AS1
4 186297569 intron variant G/A;C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs12500826
rs12500826
F11-AS1
4 186306297 intron variant T/C snv 0.60
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs149130695
rs149130695
F11-AS1
4 186464194 intron variant A/C snv 5.0E-02
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2019 2019
dbSNP: rs4444878
rs4444878
F11-AS1
0.851 0.120 4 186292729 intron variant C/A;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2016 2016
dbSNP: rs4572916
rs4572916
F11-AS1
4 186302429 intron variant A/C snv 0.22
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs907439
rs907439
F11-AS1
4 186299593 intron variant C/T snv 0.14
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011