Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1065297
CXCL12
0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02 3
rs10793538
CXCL12
1.000 0.040 10 44381138 intron variant T/A;C snv 2
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs1126742
CYP4A11
0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 4
rs11544374
APLNR
1.000 0.040 11 57237103 5 prime UTR variant C/T snv 0.21 2
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05 4
rs180070
LINC01497
0.882 0.040 17 69960745 upstream gene variant G/T snv 0.77 4
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs2280275
CYP2J2
0.925 0.040 1 59901568 intron variant T/C snv 0.23 3
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs2968915
ATP6AP2
1.000 0.040 X 40580182 intron variant G/A snv 3
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs3890011
CYP4A11
0.925 0.040 1 46933071 intron variant G/C snv 0.71 0.65 3
rs5049
AGT
1.000 0.040 1 230714337 intron variant C/T snv 0.16 3
rs553350297
AGTR1
0.882 0.040 3 148741588 missense variant G/A snv 1.2E-05 2.1E-05 4
rs56204867
APLN
0.925 0.040 X 129656490 upstream gene variant A/G snv 0.11 3
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs755559514
APLN
0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06 3
rs761401927
ACE
0.882 0.040 17 63488704 missense variant G/A snv 9.1E-05 4
rs762079672
AGT
0.882 0.040 1 230710211 missense variant C/T snv 4.0E-06 4
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 4
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5