Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 7
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs1126772
SPP1
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16 5
rs13210247
TRAF3IP2-AS1 ; TRAF3IP2
0.882 0.280 6 111601517 non coding transcript exon variant A/G snv 0.10 3
rs310241
JAK1
0.882 0.360 1 64837655 intron variant A/G snv 0.37 3
rs3818753
JAK1
1.000 0.200 1 64873549 3 prime UTR variant A/G snv 1.0E-02 3.6E-03 3
rs4073153
DNLZ ; CARD9
1.000 0.200 9 136364897 non coding transcript exon variant A/G snv 0.40 3
rs4795067
NOS2
0.882 0.280 17 27779649 intron variant A/G snv 0.31 3
rs12212193
BACH2
0.925 0.280 6 90287050 intron variant A/G snv 0.38 2
rs7028891
DELEC1
0.925 0.280 9 114882735 intron variant A/G snv 0.50 2
rs1327295035
IL17A
1.000 0.200 6 52187730 missense variant A/G snv 1
rs1522596 1.000 0.200 7 150538695 downstream gene variant A/G snv 0.47 1
rs1916012 1.000 0.200 7 150536739 intergenic variant A/G snv 0.49 1
rs224127 1.000 0.200 10 62701513 intron variant A/G snv 0.69 1
rs2834643
RUNX1
1.000 0.200 21 34814099 intron variant A/G snv 0.42 1
rs3789205
TREM1
1.000 0.200 6 41286177 intron variant A/G snv 9.4E-02 1
rs3914501
NAALADL2
1.000 0.200 3 174846878 intron variant A/G snv 0.21 1
rs855873
AIM2
1.000 0.200 1 159077922 intron variant A/G snv 0.84 1
rs9266490 1.000 0.200 6 31372381 intron variant A/G snv 0.22 1
rs936551
CPLX1
1.000 0.200 4 827702 upstream gene variant A/G snv 0.52 1
rs9517701
UBAC2
1.000 0.200 13 99377286 3 prime UTR variant A/G snv 0.13 1