Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10793538
CXCL12
1.000 0.040 10 44381138 intron variant T/A;C snv 2
rs11544374
APLNR
1.000 0.040 11 57237103 5 prime UTR variant C/T snv 0.21 2
rs948847
APLNR
1.000 0.040 11 57236870 synonymous variant G/A;T snv 0.59 2
rs1065297
CXCL12
0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02 3
rs1279844744
CYP1A1
0.925 0.080 15 74720521 missense variant A/G snv 3
rs1808593
NOS3
0.925 0.080 7 151011214 intron variant G/T snv 0.77 3
rs2280275
CYP2J2
0.925 0.040 1 59901568 intron variant T/C snv 0.23 3
rs2968915
ATP6AP2
1.000 0.040 X 40580182 intron variant G/A snv 3
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
rs56204867
APLN
0.925 0.040 X 129656490 upstream gene variant A/G snv 0.11 3
rs755559514
APLN
0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06 3
rs978906
ROCK2
0.925 0.080 2 11183150 3 prime UTR variant T/A;C snv 3
rs1126742
CYP4A11
0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 4
rs1150256
IL24
0.925 0.120 1 206899788 intron variant G/A snv 0.40 4
rs11879293
SMARCA4
0.882 0.120 19 10961934 intron variant G/A;C;T snv 4
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
rs553350297
AGTR1
0.882 0.040 3 148741588 missense variant G/A snv 1.2E-05 2.1E-05 4
rs564481
KL
0.882 0.080 13 33060846 missense variant C/A;T snv 1.2E-05; 0.38 4
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
rs3761581
APLN
0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5