Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs1558139
CYP4F2
0.851 0.160 19 15886754 intron variant G/A snv 0.46 6
rs2802292
FOXO3
0.851 0.160 6 108587315 intron variant G/T snv 0.50 6
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs2070762
TH
0.925 0.080 11 2165105 intron variant A/G snv 0.43 5
rs3785889
GOSR2 ; LRRC37A2
0.827 0.080 17 46928464 intron variant G/A snv 0.45 5
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv 4
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 4
rs6632677
ACE2
0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 4
rs743506
NOS3
0.925 0.120 7 151009827 intron variant G/A;C snv 4
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv 4
rs11572325
CYP2J2
0.925 0.080 1 59896030 intron variant A/T snv 0.12 3
rs12695895
AGTR1
0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs13306673
SLC12A3
1.000 0.040 16 56867019 intron variant C/T snv 0.10 0.13 3
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3