Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs12124383 1.000 0.080 1 155946002 downstream gene variant G/A snv 3.7E-03 2
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
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
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
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs568401628
ACE
0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 4
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
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
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
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
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
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35