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
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11048434
KLRG1
1.000 0.200 12 9001336 intron variant G/A snv 0.28 1
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs1507153 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 1
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 6
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs3823536
IRF5
0.925 0.280 7 128939612 intron variant G/A snv 0.40 2
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 5
rs9271573 1.000 0.200 6 32622724 TF binding site variant A/C snv 0.55 1
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 2
rs7999279 1.000 0.200 13 47376590 intergenic variant A/C snv 0.76 1
rs7119038 1.000 0.200 11 118867572 intergenic variant G/A snv 0.77 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59