Disease: Inflammatory Bowel Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs10063949
SLC23A1
0.882 0.080 5 139383837 intron variant T/C snv 0.48 4
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 4
rs1020856343
SLC22A5
0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104895467
NOD2
0.851 0.120 16 50716899 missense variant A/G snv 1.2E-03 7.5E-04 5
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs111456533
EEF1AKMT2
1.000 0.040 10 124750812 intron variant G/A snv 0.18 2
rs11150589
ITGAL
1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 2
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9