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: rs10025152
rs10025152
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
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
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
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
4 186306297 intron variant T/C snv 0.60
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs12644950
rs12644950
4 154616169 upstream gene variant G/A snv 0.25
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs13109457
rs13109457
4 154593727 upstream gene variant G/A snv 0.25
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs13130318
rs13130318
4 154617318 upstream gene variant T/G snv 0.23
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs1593
rs1593
F11
4 186274397 3 prime UTR variant T/A;G snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs2066861
rs2066861
FGG
4 154606284 intron variant C/T snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs2073825
rs2073825
ABO
9 133257320 intron variant A/T snv 0.25
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs2073827
rs2073827
ABO
9 133261730 intron variant G/C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs370396210
rs370396210
4 154580036 downstream gene variant -/CA delins 4.2E-05
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs3736455
rs3736455
4 186201165 synonymous variant T/A;G snv 1.6E-05; 0.59
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs3758348
rs3758348
9 133372523 intron variant G/C snv 0.13
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs4241824
rs4241824
F11
4 186270633 intron variant G/A snv 0.55
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs4572916
rs4572916
4 186302429 intron variant A/C snv 0.22
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs474279
rs474279
ABO
9 133264214 intron variant C/G;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs4962153
rs4962153
0.925 0.120 9 133458632 intron variant A/G snv 0.79
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs500428
rs500428
9 133279770 upstream gene variant G/A snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs502361
rs502361
9 133280016 upstream gene variant G/C snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs514708
rs514708
ABO
9 133258352 intron variant C/T snv 0.29
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs517414
rs517414
ABO
9 133258643 intron variant G/A snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs547643
rs547643
ABO
9 133259656 intron variant C/T snv 0.27
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011
dbSNP: rs549331
rs549331
ABO
9 133259791 intron variant C/G snv 0.28
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2011 2011