Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 4
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10