Disease: Blood Pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 6
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 5
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs11771259
C1GALT1
1.000 0.040 7 7237584 intron variant C/G snv 1.0E-01 3
rs12627514 1.000 0.040 21 43339560 intergenic variant C/A;G;T snv 3
rs12759054
SLC35F3
1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv 3
rs7733088
HTR4 ; LOC107986462
1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 3
rs11168245
HDAC7
1.000 0.040 12 47810716 intron variant C/G snv 0.16 2
rs13040716 1.000 0.040 20 32182402 downstream gene variant A/G snv 1.0E-01 2
rs1549306
CFDP1
1.000 0.040 16 75381443 intron variant T/C snv 0.52 2
rs200528
TNRC6A
1.000 0.040 16 24747810 intron variant A/G snv 0.82 2
rs229340
HSF2BP
1.000 0.040 21 43535523 intron variant T/C snv 2
rs2293947
EEFSEC
1.000 0.040 3 128378653 intron variant A/C snv 8.4E-02 2
rs305221
PKN2
1.000 0.040 1 88733302 intron variant G/A snv 0.59 2
rs36044436
GTF2I
1.000 0.040 7 74675495 intron variant C/A;G;T snv 2
rs4787486
TMEM219
1.000 0.040 16 29966241 intron variant A/T snv 0.40 2
rs55804009 1.000 0.040 18 1848628 intron variant C/A snv 0.17 2
rs61781370 1.000 0.040 1 39579628 upstream gene variant A/C snv 0.17 2
rs6799272
RSRC1
1.000 0.040 3 158470614 intron variant A/T snv 0.44 2
rs9399401
ADGRG6
1.000 0.040 6 142347764 intron variant T/C snv 0.31 2