Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16890334 6 78846449 intergenic variant T/C snv 1.9E-03 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs656319 8 9956901 intergenic variant A/G snv 0.49 3
rs7577262 2 233910224 intergenic variant G/A;T snv 4
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
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs17613287
CACNB2
10 18430748 intron variant A/T snv 0.27 4
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs17037452
CLCN6
1 11835618 intron variant A/G snv 0.18 3
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3