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
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
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
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
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
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16