Source: GWASCAT

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: rs9797861
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.710 1.000 1 2016 2016
dbSNP: rs9797861
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.710 1.000 1 2016 2016
dbSNP: rs9797861
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		0.700 1.000 1 2016 2016
dbSNP: rs9797861
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.700 1.000 1 2016 2016
dbSNP: rs9797861
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.700 1.000 1 2016 2016