Disease: Systolic Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2943646 2 226234818 intergenic variant A/C;G snv 3
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs2606736
ATG7
1.000 0.120 3 11358775 intron variant C/A;T snv 4
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12