Disease: Systolic Pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs10734252 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 3
rs11688682 1.000 0.080 2 120590036 intergenic variant G/C snv 0.20 3
rs34872471
TCF7L2
1.000 0.080 10 112994312 intron variant T/C snv 0.29 2
rs35895680 1.000 0.080 17 48982960 intergenic variant C/A snv 0.25 2