Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1887320 20 10985350 intron variant G/A snv 0.46 6
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
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
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
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs17613287
CACNB2
10 18430748 intron variant A/T snv 0.27 4
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs7577262 2 233910224 intergenic variant G/A;T snv 4
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
rs16890334 6 78846449 intergenic variant T/C snv 1.9E-03 3
rs17037452
CLCN6
1 11835618 intron variant A/G snv 0.18 3
rs1952652
LINC02227
5 158384080 intron variant A/T snv 0.28 3
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3
rs2681485
ATP2B1
12 89631845 intron variant G/A;T snv 3
rs656319 8 9956901 intergenic variant A/G snv 0.49 3