Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 7
rs2823288 0.827 0.120 21 15448569 intron variant G/A snv 0.22 5
rs4456788
GATD3A
0.827 0.120 21 44196441 intron variant G/A snv 5
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 4
rs7282490
GATD3A
0.882 0.080 21 44195858 intron variant G/A;T snv 4
rs2823286
LOC101927745
0.925 0.040 21 15445619 intron variant G/A snv 0.28 3
rs8126756
IFNGR2
0.925 0.040 21 33403138 5 prime UTR variant T/C;G snv 3
rs1297265
LOC101927745
0.925 0.040 21 15444732 intron variant A/G snv 0.44 2
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs2297441
RTEL1-TNFRSF6B ; RTEL1 ; TNFRSF6B
0.807 0.160 20 63696229 3 prime UTR variant G/A;C snv 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs6058869
DNMT3B
0.827 0.120 20 32760944 upstream gene variant C/T snv 0.55 6
rs6062496
TNFRSF6B ; RTEL1-TNFRSF6B
0.827 0.120 20 63697746 intron variant G/A snv 0.52 6
rs8124792
CYP24A1
0.827 0.120 20 54150268 downstream gene variant G/A snv 7.8E-02 6
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 6