Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs13209747 6 126794309 intron variant C/G;T snv 0.36 4
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs13405173
PDE1A
2 182449087 intron variant A/C snv 8.8E-03 3
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs1401982
ATP2B1
12 89595822 intron variant G/A snv 0.60 4
rs1407040
GNAS
20 58897119 intron variant C/T snv 0.70 4
rs1446468 2 164106976 intron variant T/C snv 0.40 3
rs145485557
POC1B
12 89445110 intron variant C/T snv 4.7E-02 4
rs1502284
ARHGAP42
11 100713419 intron variant T/A;G snv 2
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 3
rs1563788
ZNF318
6 43340625 intron variant C/T snv 0.42 4
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs16849225 2 164050310 intron variant C/T snv 0.19 4
rs17004869
FGF5
4 80283879 intron variant A/T snv 4.6E-02 4
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs17135875
FBXL13
7 102878584 intron variant T/C snv 0.24 3
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 4
rs1731243
KCNK3
2 26707543 intron variant C/T snv 0.48 4
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 4
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5