Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17490626
TSPAN15
0.882 0.120 10 69458890 intron variant G/C snv 8.4E-02 5
rs1864169
GTF2A1 ; SNORA79
0.851 0.200 14 81203689 intron variant G/T snv 0.78 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs34234989
MMP24-AS1-EDEM2 ; PROCR
0.882 0.120 20 35186731 intron variant A/- delins 0.40 5
rs3787268
MMP9 ; SLC12A5-AS1
0.851 0.240 20 46013092 intron variant G/A;T snv 5
rs3826392
ZNF18 ; MAP2K4
0.827 0.200 17 12019587 intron variant G/T snv 0.65 5
rs4769874
ALOX5AP
0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs548987
SLC17A3
0.882 0.200 6 25869143 intron variant G/C snv 0.20 5
rs7217186
ALOX15
0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs72798544
COX7A2L
0.882 0.120 2 42372465 intron variant T/G snv 1.3E-02 5
rs7950273
PDGFD
0.925 0.120 11 104160870 intron variant C/G snv 0.32 5
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs11634042
ADAMTS7 ; MORF4L1
0.882 0.120 15 78813008 intron variant C/T snv 0.33 4
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 4
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs161810
TNFRSF9
0.925 0.120 1 7940737 intron variant T/C snv 0.13 4
rs243327
RMI2 ; LOC105371082
0.882 0.280 16 11259447 intron variant A/G snv 0.52 4
rs3212335
GABRB3 ; LOC112268151
1.000 0.080 15 26766994 intron variant C/T snv 0.32 4
rs4073259
ALOX5AP
0.882 0.160 13 30732134 intron variant G/A snv 0.49 4
rs4376531
ARHGEF10
0.925 0.120 8 1906652 intron variant C/A;G snv 4
rs6632677
ACE2
0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 4
rs11984041
HDAC9
0.925 0.080 7 18992312 intron variant C/T snv 0.13 3
rs1324214
F3
0.925 0.120 1 94531732 intron variant G/A snv 0.21 3