Disease: Blood Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs11105354
ATP2B1
12 89632746 intron variant A/G snv 0.15 3
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs1156725
SOX6
11 16286154 intron variant C/T snv 0.78 3
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
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
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
rs1421811
NPR3
5 32714164 intron variant C/G;T snv 2
rs1446468 2 164106976 intron variant T/C snv 0.40 4
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 6
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5