Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
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
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs7823056 8 8525195 intergenic variant A/G snv 0.55 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6