Disease: Diastolic 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
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6