Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv 5
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2681485
ATP2B1
12 89631845 intron variant G/A;T snv 3
rs7577262 2 233910224 intergenic variant G/A;T snv 4
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs16890334 6 78846449 intergenic variant T/C snv 1.9E-03 3
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3