Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs17004869
FGF5
4 80283879 intron variant A/T snv 4.6E-02 4
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs1731243
KCNK3
2 26707543 intron variant C/T snv 0.48 4
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs186208701
STK3
8 98567888 intron variant T/C snv 3.3E-03 3
rs187821766
STK3
8 98729050 intron variant C/T snv 3.5E-03 3
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1902859 4 80236549 regulatory region variant T/C snv 0.27 4
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2021783
TNXB
6 32077074 intron variant C/T snv 1.0E-02 3
rs2240736
TBX2
17 61408032 non coding transcript exon variant C/T snv 0.64 0.68 4
rs2270860
SLC22A7 ; CRIP3
6 43302413 splice region variant C/T snv 0.37 0.43 4
rs2493134
AGT
1 230713613 intron variant T/C snv 0.57 4
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs2649044
SWAP70
11 9742422 intron variant C/T snv 0.55 4
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs35021474
KCNK3
2 26693976 intron variant C/G snv 0.48 4
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs35529250
RBM47
4 40426074 missense variant C/G;T snv 1.2E-05; 3.7E-03 3
rs3774427
CACNA1D
3 53531601 intron variant C/G snv 0.11 4
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5