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: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs11105354
rs11105354
12 89632746 intron variant A/G snv 0.15
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs11160059
rs11160059
14 92340986 intron variant T/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs11222084
rs11222084
11 130403335 non coding transcript exon variant A/T snv 0.30
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1156725
rs1156725
11 16286154 intron variant C/T snv 0.78
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs11659639
rs11659639
18 60500379 intron variant T/G snv 1.1E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1173756
rs1173756
5 32789746 3 prime UTR variant T/C snv 0.56 0.60
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1173766
rs1173766
5 32804422 intergenic variant T/C snv 0.57
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1173771
rs1173771
5 32814922 regulatory region variant A/G snv 0.65
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs12098903
rs12098903
11 55899037 downstream gene variant A/T snv 5.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs12098904
rs12098904
11 55899077 downstream gene variant A/T snv 5.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
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: 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: 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: 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: 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