Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs17613287
CACNB2
10 18430748 intron variant A/T snv 0.27 4
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs1952652
LINC02227
5 158384080 intron variant A/T snv 0.28 3
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs656319 8 9956901 intergenic variant A/G snv 0.49 3
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5