Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs9838915
KLF15
0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs2149954
LINC02227
0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs7521023
CASQ2
1.000 0.040 1 115700759 3 prime UTR variant G/A snv 0.64 2
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54