Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv 5
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs1952652
LINC02227
5 158384080 intron variant A/T snv 0.28 3
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3