Disease: Blood Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 9
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs7733088
HTR4 ; LOC107986462
1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 5
rs9399401
ADGRG6
1.000 0.040 6 142347764 intron variant T/C snv 0.31 4