Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 2
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 6
rs3823536
IRF5
0.925 0.280 7 128939612 intron variant G/A snv 0.40 2
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs6579837
TNIP1
1.000 0.200 5 151055333 intron variant G/T snv 0.11 1
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs7119038 1.000 0.200 11 118867572 intergenic variant G/A snv 0.77 1
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs7999279 1.000 0.200 13 47376590 intergenic variant A/C snv 0.76 1
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs9271573 1.000 0.200 6 32622724 TF binding site variant A/C snv 0.55 1
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs9938751
SHISA9
1.000 0.200 16 12908502 missense variant T/A;C snv 0.88 1