Disease: Diastolic blood pressure measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 4
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 3
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 3
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs9815354
ULK4
0.925 0.160 3 41871159 intron variant G/A;T snv 3
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 2
rs1918974
MECOM-AS1 ; MECOM
1.000 0.040 3 169448100 intron variant C/T snv 0.57 2
rs2384550 1.000 0.040 12 114914926 regulatory region variant G/A snv 0.33 2