Source: GWASDB

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: rs5030091
rs5030091
KNG1
3 186743088 3 prime UTR variant T/C snv 0.42
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.700 1.000 1 2013 2013
dbSNP: rs651007
rs651007 		0.851 0.160 9 133278431 upstream gene variant T/A;C snv
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.700 1.000 1 2013 2013
dbSNP: rs657152
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.700 1.000 1 2013 2013
dbSNP: rs7381103
rs7381103
F12 ; GRK6 ; SLC34A1
5 177411311 intron variant C/G snv 0.11
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.700 1.000 1 2013 2013
dbSNP: rs7447593
rs7447593
SLC34A1
5 177397136 non coding transcript exon variant C/G;T snv
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2545801
rs2545801
GRK6
5 177414338 intron variant T/C snv 0.56
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.800 1.000 2 2012 2013
dbSNP: rs710446
rs710446
KNG1
0.925 0.120 3 186742138 missense variant T/C snv 0.42 0.44
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.800 1.000 3 2010 2013
dbSNP: rs9898
rs9898
HRG ; LOC105374258
0.925 0.160 3 186672838 missense variant C/T snv 0.38 0.43
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.800 1.000 3 2010 2013