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: rs11191593
rs11191593
10 103179458 intron variant T/C snv 9.0E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 2 2011 2013
dbSNP: rs1421811
rs1421811
5 32714164 intron variant C/G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 2 2011 2014
dbSNP: rs10143078
rs10143078
14 70414772 intron variant A/C snv 6.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2014 2014
dbSNP: rs10197121
rs10197121
2 10153562 intron variant C/T snv 0.64
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs10444602
rs10444602
12 131708291 upstream gene variant T/G snv 0.51
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs10555137
rs10555137
8 127457345 intron variant C/T snv 6.6E-02
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: rs11816631
rs11816631
10 97802815 intergenic variant A/G snv 8.8E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2014 2014
dbSNP: rs12067906
rs12067906
1 192462868 intron variant T/C snv 0.12
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.800 1.000 1 2012 2012
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: 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: rs1223397
rs1223397
6 13270713 intron variant G/A;C snv 0.19
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.800 1.000 1 2012 2012
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