Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801483
GCGR
0.851 0.160 17 81809839 missense variant G/A snv 7.4E-03 6.3E-03 7
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs225015
DIO2
0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 6
rs2285666
ACE2
0.925 0.160 X 15592225 splice region variant C/T snv 6.2E-06; 0.28 0.23 4
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs1801273
FABP1
0.925 0.200 2 88126256 missense variant C/T snv 1.2E-05 2.1E-05 3
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05 5
rs201739205
LOC108783654 ; HSD17B1
0.851 0.200 17 42552898 5 prime UTR variant A/C snv 7.8E-03 8.2E-03 5
rs2266782
FMO3
0.851 0.200 1 171107825 missense variant G/A snv 0.37 0.41 7
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03 5