Disease: Systolic 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
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
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
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
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs3741210
INS-IGF2 ; IGF2 ; IGF2-AS
11 2148310 non coding transcript exon variant A/G snv 0.30 2