Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs10504249
LINC01602 ; LOC105375856
8 57876522 intron variant A/G snv 1.7E-02 3
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
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
rs10948071
ZNF318
6 43312975 intron variant C/T snv 0.46 4
rs1105955 6 126826023 intron variant T/A snv 0.44 3
rs1105956 6 126825734 intron variant G/A snv 0.44 2
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11105352
ATP2B1
12 89632685 intron variant G/A snv 0.14 4
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs111478946
ATP2B1
12 89665065 intron variant G/A snv 0.14 4
rs11191871
LOC102724351
10 103947673 intergenic variant A/G snv 5.2E-02 2
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
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs1173766 5 32804422 intergenic variant T/C snv 0.57 3
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs1177765 5 32829823 intergenic variant T/C snv 0.50 3
rs11867410
APOH
17 66231245 intron variant T/C snv 4.0E-02 3
rs11887188 2 234394166 intergenic variant C/T snv 0.11 3
rs12118370
ST7L
1 112605645 intron variant A/G snv 0.24 3
rs12129649
MOV10
1 112688881 5 prime UTR variant G/T snv 6.6E-02 4