Disease: Blood Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10143078
COX16 ; SYNJ2BP-COX16 ; SYNJ2BP
14 70414772 intron variant A/C snv 6.6E-02 2
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs11105354
ATP2B1
12 89632746 intron variant A/G snv 0.15 3
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs11222084
ZBTB44-DT
11 130403335 non coding transcript exon variant A/T snv 0.30 3
rs1156725
SOX6
11 16286154 intron variant C/T snv 0.78 3
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs12195230
KLHL32
6 97052171 intron variant G/C snv 0.23 2
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 5
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs13002573 2 164058698 intron variant A/G snv 0.20 3
rs13082711 3 27496418 intergenic variant T/C snv 0.16 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1401454
SOX6
11 16228637 intron variant C/A;G;T snv 3