Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11712619
KALRN
0.882 0.160 3 124300955 intron variant C/A;T snv 0.26 5
rs225015
DIO2
0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 5
rs7950273
PDGFD
0.925 0.120 11 104160870 intron variant C/G snv 0.32 5
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs1057518903
MEN1
0.882 0.160 11 64807890 splice region variant C/- delins 6
rs619203
ROS1
0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 6
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 7
rs1801483
GCGR
0.851 0.160 17 81809839 missense variant G/A snv 7.4E-03 6.3E-03 7
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs55951658
CYP3A4
0.827 0.200 7 99770202 missense variant T/A;C snv 4.1E-04 9.8E-05 7
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs2281939
SORBS1
0.790 0.320 10 95414595 missense variant T/C snv 8.2E-02 0.13 9
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10