Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 6
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 4
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 3
rs111245230
SVEP1
1.000 0.040 9 110407495 missense variant T/C snv 2.6E-02 2.3E-02 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3