Disease: Systolic Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10062049 5 62258054 regulatory region variant C/T snv 0.16 2
rs10077885 5 115054424 regulatory region variant C/A snv 0.56 2
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10628234 15 74918801 downstream gene variant -/CA delins 2
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs1105955 6 126826023 intron variant T/A snv 0.44 3
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 8
rs11145807 9 136626337 regulatory region variant A/G snv 0.50 2
rs112204826 21 43301147 TF binding site variant C/T snv 2.9E-02 2
rs113161639 3 154898030 intergenic variant G/T snv 7.3E-02 2
rs11486794 7 2452283 downstream gene variant C/T snv 0.14 2
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs11563582 7 27312031 intergenic variant G/A snv 9.8E-02 3
rs115893283 20 56829109 intergenic variant C/T snv 4.8E-02 2
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs1177765 5 32829823 intergenic variant T/C snv 0.50 3
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs11993898 8 51024072 intergenic variant T/A;C snv 2
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16