Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs218966
PHF14
7 10982603 missense variant A/G snv 0.64 0.68 2
rs3851059 10 80270902 downstream gene variant G/A snv 0.27 2
rs2132572
IGFBP3
1.000 7 45921946 upstream gene variant T/C snv 0.79 3
rs2301339
CDCA3 ; GNB3
1.000 0.080 12 6845460 3 prime UTR variant G/A;T snv 3
rs4471613
ALDH1A2
1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02 3
rs650439
KL
1.000 0.080 13 33061802 intron variant T/A snv 0.82 0.81 3
rs7087728
MAT1A
10 80273714 3 prime UTR variant G/A;C snv 3
rs17809012
CCL11
0.925 0.160 17 34285425 upstream gene variant A/G;T snv 4
rs7201
MMP2
0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37 4
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs2230500
PRKCH
0.925 0.080 14 61457521 missense variant G/A snv 3.1E-02 1.6E-02 5
rs852426
ACTB
0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs2266782
FMO3
0.851 0.200 1 171107825 missense variant G/A snv 0.37 0.41 7
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs7136446
IGF1 ; LINC02456
0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs2266780
FMO3
0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10