Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999788
IL10RB ; IL10RB-DT ; IFNAR2
0.925 0.120 21 33265726 non coding transcript exon variant C/T snv 0.20 2
rs9920
CAV1
1.000 0.040 7 116560038 3 prime UTR variant T/C snv 6.7E-02 3
rs9884090
ARHGAP31
1.000 0.040 3 119397303 intron variant G/A snv 0.15 1
rs987870
HLA-DPA1 ; HLA-DPB1
0.851 0.160 6 33075103 intron variant A/G snv 0.19 4
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 5
rs959173
CAV1
0.925 0.120 7 116542000 intron variant C/T snv 0.78 2
rs9373839
ATG5
0.882 0.080 6 106207742 intron variant T/C snv 0.15 3
rs936469
PHRF1
1.000 0.040 11 606749 non coding transcript exon variant G/A snv 0.24 1
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs9275390 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 3
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs9275245 0.925 0.160 6 32693166 intergenic variant A/G;T snv 2
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 3
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs883770
GSDMB
1.000 0.040 17 39907128 non coding transcript exon variant C/G;T snv 1
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs8182352 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 5
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs798036
CD2
1.000 0.040 1 116766208 intron variant T/A snv 0.17 1
rs7934606
MUC2
1.000 0.040 11 1100037 intron variant C/G;T snv 2
rs7929541 0.851 0.160 11 633689 upstream gene variant T/C snv 0.34 4
rs7900522
LRMDA
1.000 0.040 10 76350213 intron variant T/A;C snv 1