Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1952652
LINC02227
5 158384080 intron variant A/T snv 0.28 3
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681485
ATP2B1
12 89631845 intron variant G/A;T snv 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv 5
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
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs656319 8 9956901 intergenic variant A/G snv 0.49 3
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs7577262 2 233910224 intergenic variant G/A;T snv 4