Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 5
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs7823056 8 8525195 intergenic variant A/G snv 0.55 3
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
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
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 4
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4