Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6590811
ARHGAP42
11 100708153 intron variant C/T snv 0.53 4
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs6590816
ARHGAP42
11 100730902 intron variant G/A snv 0.40 4
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs13175330
PAM
5 102840757 intron variant A/G snv 7.8E-02 2
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs12046278
CASZ1
1 10739520 intron variant T/C snv 0.36 3
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs12129649
MOV10
1 112688881 5 prime UTR variant G/T snv 6.6E-02 4
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs35444 12 115114632 intergenic variant A/G snv 0.38 6