Disease: Ulcerative Colitis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 4
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs2297441
RTEL1-TNFRSF6B ; RTEL1 ; TNFRSF6B
0.807 0.160 20 63696229 3 prime UTR variant G/A;C snv 2
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 2
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 2
rs9822268
APEH
0.925 0.040 3 49682296 intron variant G/A;T snv 2
rs9858542
BSN
0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 2