Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs1878672
IL19 ; IL10
0.882 0.080 1 206770368 intron variant G/A;C;T snv 3
rs3024491
IL19 ; IL10
0.925 0.040 1 206771701 intron variant C/A;T snv 2
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs2072493
TLR5
0.851 0.280 1 223111257 missense variant T/A;C snv 0.16 4
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs17163737
TLR5
0.882 0.120 1 223129809 intron variant G/T snv 7.2E-02 3
rs1640827
TLR5
0.882 0.120 1 223138265 intron variant C/G;T snv 3
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs2075820
NOD1
0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs2709800
NOD1
0.882 0.120 7 30473155 intron variant A/C snv 0.53 4
rs2015620
IL32
0.882 0.120 16 3073560 intron variant A/G;T snv 3
rs2376549
DEFB121
0.925 0.120 20 31411284 intron variant C/T snv 0.42 2
rs6912200
PGC
0.925 0.080 6 41750170 intron variant C/T snv 0.54 3
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs2243086
CHRNE ; GP1BA
1.000 0.040 17 4930914 intron variant G/T snv 0.20 2
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs2066842
NOD2
0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs7205423
LOC102724907
1.000 0.040 16 50735351 intron variant C/G;T snv 1
rs718226
LOC102724907
0.882 0.120 16 50735652 intron variant A/G snv 0.36 4
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105