Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs4936742
UBASH3B
0.925 0.200 11 122770378 intron variant T/C snv 0.64 2
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs5743733
TLR7
0.925 0.280 X 12871589 intron variant C/G;T snv 2
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs3853839
TLR7
0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 10
rs752637
IRF5
0.925 0.280 7 128939366 intron variant T/A;C snv 2
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs76481776
MIR182 ; LOC105375501
0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02 4
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs4073153
DNLZ ; CARD9
1.000 0.200 9 136364897 non coding transcript exon variant A/G snv 0.40 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs9494885
LOC107986649 ; WAKMAR2
0.882 0.320 6 137851611 intron variant T/C snv 0.20 3
rs7753873
LOC107986649 ; WAKMAR2
0.882 0.320 6 137852285 intron variant A/C snv 0.18 3
rs10277380 1.000 0.200 7 150533604 intergenic variant T/A;C snv 1
rs11769828 1.000 0.200 7 150534221 intergenic variant C/T snv 0.19 1
rs1916012 1.000 0.200 7 150536739 intergenic variant A/G snv 0.49 1
rs1522596 1.000 0.200 7 150538695 downstream gene variant A/G snv 0.47 1
rs10236188 1.000 0.200 7 150548168 intergenic variant T/C snv 0.49 1
rs1608157
LOC107986860
1.000 0.200 7 150549936 intergenic variant C/G;T snv 1
rs10256482 1.000 0.200 7 150653887 intergenic variant T/C snv 0.47 1