Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs7119038 1.000 0.200 11 118867572 intergenic variant G/A snv 0.77 1
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
rs17339836
TNPO3
1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 1
rs9938751
SHISA9
1.000 0.200 16 12908502 missense variant T/A;C snv 0.88 1
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs6579837
TNIP1
1.000 0.200 5 151055333 intron variant G/T snv 0.11 1
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 2
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs10553577
STAT4
1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3135394
HLA-DRA
0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4
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
rs115575857 1.000 0.200 6 32691868 regulatory region variant A/G snv 1