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
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs56394279
B3GAT3P1 ; TRIM59-IFT80 ; TRIM59
3 160453304 non coding transcript exon variant C/A;T snv 3