Disease: Diastolic blood pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs1407040
GNAS
20 58897119 intron variant C/T snv 0.70 4
rs28362590
RAB24 ; PRELID1 ; MXD3
5 177304451 intron variant G/C;T snv 0.78 2