Disease: Systolic Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16