Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1567438
LPAL2
0.925 0.200 6 160458599 intron variant T/C snv 0.25 3
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11538209
ALB
1.000 0.120 4 73404356 missense variant T/C snv 2
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11643718
SLC12A3
0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 10
rs1177506410
AGT
0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 12
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73