Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 5
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
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
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7