Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1105956 6 126825734 intron variant G/A snv 0.44 2
rs11191871
LOC102724351
10 103947673 intergenic variant A/G snv 5.2E-02 2
rs12209106 6 1620807 downstream gene variant T/G snv 0.37 2
rs12579720
LINC02398
12 20020830 intron variant C/A;G;T snv 2
rs1502284
ARHGAP42
11 100713419 intron variant T/A;G snv 2
rs16833934 3 164019462 intergenic variant A/G snv 0.34 2
rs2048765
HDAC4
2 239286459 intron variant A/G snv 9.6E-02 2
rs2881854
ENPEP
4 110422107 intron variant C/A snv 0.83 2
rs3118867
DAPK1
9 87646780 intron variant A/G snv 0.41 2
rs3774447
CACNA1D
3 53561685 intron variant T/C snv 2.9E-02 2
rs4494250
CYP2C19
10 94804000 intron variant G/A snv 0.28 2
rs58190593
BORCS8-MEF2B ; MEF2B
19 19153129 intron variant C/T snv 0.16 2
rs603788
KCNMA1
10 77451504 intron variant G/C snv 0.46 2
rs6658555
ST7L
1 112555912 missense variant C/T snv 0.19 0.20 2
rs6772151
MYL3
3 46855009 intron variant C/A;G;T snv 2
rs75483173 2 163587909 intergenic variant A/G;T snv 2
rs75746498
MEF2B ; BORCS8-MEF2B
19 19149877 intron variant G/A;C;T snv 2
rs7928655
ARNTL
11 13278705 intron variant C/G snv 0.61 2
rs10504249
LINC01602 ; LOC105375856
8 57876522 intron variant A/G snv 1.7E-02 3
rs10897164
LRRC10B
11 61510303 3 prime UTR variant A/G snv 0.13 3
rs10930597 2 173462117 intergenic variant C/T snv 0.14 3
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 3
rs1105955 6 126826023 intron variant T/A snv 0.44 3
rs112640876
LSP1
11 1873813 intron variant A/G;T snv 3
rs112862634
LINC00461 ; MEF2C-AS2
5 88674534 intron variant G/C snv 0.17 3