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: rs12098941
rs12098941
11 55898967 downstream gene variant T/A;G snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs12195036
rs12195036
6 166038209 intergenic variant T/C snv 4.1E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2014 2014
dbSNP: rs12195230
rs12195230
6 97052171 intron variant G/C snv 0.23
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2014 2014
dbSNP: rs12258967
rs12258967
10 18439030 intron variant C/G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs12279202
rs12279202
11 9410543 intron variant C/T snv 4.8E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs12416687
rs12416687
10 102869254 intron variant T/C snv 0.21
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2014 2014
dbSNP: rs12940887
rs12940887
17 49325445 intron variant C/T snv 0.28
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs12946454
rs12946454
0.925 0.040 17 45130754 intron variant A/T snv 0.21
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs13002573
rs13002573
2 164058698 intron variant A/G snv 0.20
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs13082711
rs13082711
3 27496418 intergenic variant T/C snv 0.16
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs13107325
rs13107325
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs13139571
rs13139571
1.000 0.040 4 155724361 intron variant C/A snv 0.22
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs13149993
rs13149993
4 80237391 regulatory region variant G/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs13209747
rs13209747
6 126794309 intron variant C/G;T snv 0.36
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2013 2013
dbSNP: rs1327235
rs1327235
20 10988382 intron variant A/G snv 0.46
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs13306560
rs13306560
1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2010 2010
dbSNP: rs13424629
rs13424629
2 10156359 intron variant T/C snv 0.15
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1343040
rs1343040
3 169468505 intron variant G/A snv 0.36
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1384089
rs1384089
11 56081540 upstream gene variant G/C snv 6.0E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1401454
rs1401454
11 16228637 intron variant C/A;G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2013 2013
dbSNP: rs1446468
rs1446468
2 164106976 intron variant T/C snv 0.40
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1458038
rs1458038
0.925 0.120 4 80243569 intergenic variant C/T snv 0.23
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1476413
rs1476413
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1492840
rs1492840
4 45764988 intergenic variant A/C;G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1595373
rs1595373
11 16245194 intron variant G/A snv 0.78
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011