Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs3785356
IL4R
0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10494132
CHIA
0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs11071559
RORA
0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs1805014
IL4R
0.851 0.080 16 27363708 missense variant T/C snv 7.4E-03 1.4E-02 4
rs1999071 0.851 0.080 14 22659998 regulatory region variant T/C snv 0.29 4
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 4
rs2073643
SLC22A5
1.000 0.080 5 132387596 intron variant T/C snv 0.46 4
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs3742030
TRPV4
0.925 0.080 12 109814742 missense variant G/A;C snv 3.7E-02 4
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs4253238
KLKB1
0.925 0.080 4 186227233 intron variant C/T snv 0.59 4
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4