Disease: Systolic Pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 8
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 5
rs2305013
ARHGEF12
11 120469351 missense variant A/G;T snv 6.2E-02 4.2E-02 3
rs76020419
ANGPT2 ; MCPH1
8 6502768 3 prime UTR variant G/T snv 2.7E-02 2
rs786906
PKN2
1 88805891 splice region variant T/C snv 0.56 0.51 2