Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs316019
SLC22A2
0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs1801483
GCGR
0.851 0.160 17 81809839 missense variant G/A snv 7.4E-03 6.3E-03 7
rs2746071
RGS2
0.882 0.160 1 192808434 intron variant A/G snv 0.35 4
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 4
rs1567438
LPAL2
0.925 0.200 6 160458599 intron variant T/C snv 0.25 3
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 2