Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7823056 8 8525195 intergenic variant A/G snv 0.55 3
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 4
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 5
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs1327235 20 10988382 intron variant A/G snv 0.46 7