Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1808593
NOS3
0.925 0.080 7 151011214 intron variant G/T snv 0.77 3
rs2026458
PHACTR1
0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2280275
CYP2J2
0.925 0.040 1 59901568 intron variant T/C snv 0.23 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs2968915
ATP6AP2
1.000 0.040 X 40580182 intron variant G/A snv 3
rs3890011
CYP4A11
0.925 0.040 1 46933071 intron variant G/C snv 0.71 0.65 3
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs5049
AGT
1.000 0.040 1 230714337 intron variant C/T snv 0.16 3