Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs3020314
ESR1
0.790 0.280 6 151949537 intron variant C/G;T snv 7
rs3212961
ERCC1
0.827 0.200 19 45419065 intron variant G/A;T snv 1.9E-04; 0.20 7
rs4937362
LOC105369568
0.827 0.240 11 128622844 intron variant T/C snv 0.49 5
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24 4
rs3117222
HLA-DPA2
0.882 0.280 6 33093172 intron variant C/T snv 0.33 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs2855429
COL11A2
0.925 0.120 6 33190412 intron variant A/C snv 0.78 2
rs3789068
MIR4435-2HG ; BCL2L11
0.925 0.120 2 111151670 intron variant A/G snv 0.41 2
rs6444305
LPP
0.925 0.120 3 188582114 intron variant G/A;C;T snv 2
rs1493202
XKR9
1.000 0.120 8 70993352 intron variant T/G snv 0.41 1
rs28530648
HLA-DRB6
1.000 0.120 6 32559302 intron variant A/C;T snv 1
rs2894253
TSBP1-AS1
1.000 0.120 6 32377763 intron variant T/G snv 1.0E-01 1
rs4760655
VDR
1.000 0.120 12 47900348 intron variant G/A snv 0.72 1
rs9274614
HLA-DQB1
1.000 0.120 6 32668069 intron variant C/A;G snv 1
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4
rs17749561 0.925 0.120 18 63115978 intergenic variant G/A snv 5.9E-02 2
rs9275245 0.925 0.160 6 32693166 intergenic variant A/G;T snv 2
rs28605404
HLA-DRB1
1.000 0.120 6 32601910 intergenic variant A/G snv 0.10 1
rs28895078 1.000 0.120 6 32450114 intergenic variant C/A;G snv 0.13 1
rs28895103 1.000 0.120 6 32451687 intergenic variant G/A snv 0.13 1