Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs7183955
RORA
0.925 0.080 15 60757370 intron variant A/C snv 0.24 2
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs28635831
COG6
0.925 0.080 13 39745817 intron variant A/G snv 0.27 2
rs6866614
IRF1-AS1
0.925 0.080 5 132451445 intron variant A/G snv 0.71 2
rs12788104 1.000 11 1129831 regulatory region variant A/G snv 0.55 1
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 3
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs3024655
IL4R
0.925 0.080 16 27358181 intron variant A/G;T snv 2
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27 2
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs56389811
HDAC7
1.000 12 47811575 intron variant C/A;T snv 1
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4