Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs12952581
LOC102724596
0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs1655558
ITPKA
0.925 0.080 15 41495387 intron variant T/G snv 0.66 3
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs28406364
LOC102724596
1.000 0.080 17 49377145 intron variant C/T snv 0.33 3
rs449454
NDFIP1
0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3
rs6461503 0.925 0.080 7 20521373 intergenic variant T/C;G snv 3
rs7625643
ZBTB38
0.925 0.080 3 141431184 intron variant A/G snv 0.51 3
rs7626218
TBL1XR1
0.925 0.080 3 177134250 intron variant A/T snv 0.41 3
rs7734635 0.925 0.080 5 110823145 intergenic variant A/G snv 0.30 3
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34 3