Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs2276047
INPPL1
1.000 0.040 11 72230337 intron variant A/G snv 0.28 0.33 3
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs6978712
LOC105375490
1.000 0.040 7 127507709 intergenic variant C/T snv 0.11 3
rs7539020
AGT
1.000 0.040 1 230713444 intron variant C/T snv 0.43 3
rs7690819 1.000 0.040 4 111199502 intergenic variant A/G;T snv 3
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs1873077
CNTN3
0.925 0.080 3 74273636 intron variant T/C snv 0.24 4
rs7528153
VAV3
0.925 0.080 1 107765105 missense variant T/A snv 0.58 0.64 4
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
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
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1269801977
PPIG
0.925 0.120 2 169604087 missense variant A/G snv 4.0E-06 7.0E-06 4
rs17118
XYLB
0.925 0.120 3 38362981 missense variant C/A;T snv 0.29 4
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs7950273
PDGFD
0.925 0.120 11 104160870 intron variant C/G snv 0.32 5
rs11712619
KALRN
0.882 0.160 3 124300955 intron variant C/A;T snv 0.26 5
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 7