Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2285666
ACE2
0.925 0.160 X 15592225 splice region variant C/T snv 6.2E-06; 0.28 0.23 4
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 4
rs852426
ACTB
0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35