Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17613287
CACNB2
10 18430748 intron variant A/T snv 0.27 4
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
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
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs2681485
ATP2B1
12 89631845 intron variant G/A;T snv 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
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
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3
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
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
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