Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs2066715
ABCA1
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs72653706
ABCC6
0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05 4
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs761401927
ACE
0.882 0.040 17 63488704 missense variant G/A snv 9.1E-05 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
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
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