Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs10930597 2 173462117 intergenic variant C/T snv 0.14 3
rs1105955 6 126826023 intron variant T/A snv 0.44 3
rs1105956 6 126825734 intron variant G/A snv 0.44 2
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs1173766 5 32804422 intergenic variant T/C snv 0.57 3
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs1177765 5 32829823 intergenic variant T/C snv 0.50 3
rs11887188 2 234394166 intergenic variant C/T snv 0.11 3
rs12209106 6 1620807 downstream gene variant T/G snv 0.37 2
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs13082711 3 27496418 intergenic variant T/C snv 0.16 3
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 4
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs1330225 1 106293321 intergenic variant T/C snv 0.38 3
rs138088171 8 142938855 intergenic variant C/T snv 0.34 3
rs1446468 2 164106976 intron variant T/C snv 0.40 3