Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11018628
NOX4
1.000 0.080 11 89473343 intron variant T/C;G snv 2
rs1481280
ROCK1
1.000 0.080 18 21075490 intron variant C/A snv 0.31 2
rs1671021
LLGL2
1.000 0.080 17 75569090 missense variant T/C snv 0.36 0.50 2
rs17286604
KALRN
1.000 0.080 3 124233370 intron variant C/T snv 0.28 2
rs322931
LINC01221
1.000 0.080 1 199050726 intron variant G/A snv 0.22 2
rs4499545
ROPN1
1.000 0.080 3 123986995 intron variant G/A snv 0.18 2
rs7589629
ROCK2
1.000 0.080 2 11233081 intron variant G/T snv 0.44 2
rs866528738
POU2F3
1.000 0.080 11 120302360 missense variant G/A snv 2
rs147783135
TMPRSS7
1.000 0.080 3 112081004 stop gained C/T snv 2.4E-04 6.3E-05 3
rs191885206
CYP4F12
1.000 0.080 19 15696024 missense variant T/C snv 7.0E-04 3.1E-04 3
rs2292661
PDIA5
1.000 0.080 3 123150263 missense variant C/G;T snv 8.2E-04 3
rs4471613
ALDH1A2
1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02 3
rs5335
EDNRA
0.925 0.120 4 147542688 3 prime UTR variant G/A;C snv 3
rs768349387
ADRB2
1.000 0.080 5 148827850 missense variant T/C snv 8.0E-06 3
rs796145467
LDLR
0.925 0.080 19 11123310 synonymous variant C/T snv 4.0E-06 2.1E-05 3
rs876537
CRPP1
1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 3
rs978906
ROCK2
0.925 0.080 2 11183150 3 prime UTR variant T/A;C snv 3
rs10489177
C1orf112 ; METTL18
0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs1057293
SGK1
0.925 0.120 6 134172259 synonymous variant G/A snv 0.12 0.11 4
rs17118
XYLB
0.925 0.120 3 38362981 missense variant C/A;T snv 0.29 4
rs243327
RMI2 ; LOC105371082
0.882 0.280 16 11259447 intron variant A/G snv 0.52 4
rs3212335
GABRB3 ; LOC112268151
1.000 0.080 15 26766994 intron variant C/T snv 0.32 4
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs11712619
KALRN
0.882 0.160 3 124300955 intron variant C/A;T snv 0.26 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5