Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12507813 1.000 0.040 4 165013422 upstream gene variant G/A;C;T snv 1
rs12551356 1.000 0.040 9 74698280 intergenic variant G/T snv 0.11 1
rs12944194 1.000 0.040 17 73850424 intergenic variant T/C snv 0.63 1
rs12730735
AP4B1-AS1 ; PTPN22
1.000 0.040 1 113838835 intron variant T/C snv 0.21 1
rs75201096
GNA14-AS1 ; GNA14
1.000 0.040 9 77483984 intron variant T/C snv 1.6E-02 1
rs9606615
IL17RA
1.000 0.040 22 17099923 intron variant T/C snv 0.41 1
rs791903
IP6K3
1.000 0.040 6 33734868 intron variant G/C snv 0.53 1
rs165501
IRAK2
1.000 0.040 3 10167559 intron variant T/A;C snv 1
rs3027452
MAOB
1.000 0.040 X 43798542 intron variant G/A snv 0.13 1
rs2009895
SELENOS
1.000 0.040 15 101276024 intron variant C/A;T snv 3.0E-02 1
rs9607715
SGSM3
1.000 0.040 22 40399790 intron variant G/A snv 3.4E-02 1
rs2298213
TNFRSF18
1.000 0.040 1 1203822 synonymous variant T/C snv 9.1E-02 0.17 1
rs6972286 1.000 0.040 7 118685680 intergenic variant A/T snv 0.43 2
rs7178239 1.000 0.040 15 101267907 downstream gene variant C/G snv 0.37 2
rs977706 1.000 0.040 17 13456118 intergenic variant A/T snv 0.13 2
rs756763
CA10
1.000 0.040 17 51671952 intron variant A/G snv 0.48 2
rs2569192
CD14 ; TMCO6
0.925 0.120 5 140635623 upstream gene variant G/C snv 0.27 2
rs327463
CEP128
0.925 0.120 14 80784911 missense variant T/C;G snv 0.38; 4.1E-06 2
rs1269486
GATA3 ; GATA3-AS1 ; LOC107984204
0.925 0.120 10 8054236 intron variant A/G snv 0.77 2
rs2184658
HLX-AS1 ; HLX
0.925 0.120 1 220879115 intron variant C/G snv 0.20 2
rs2227478
IL22 ; LOC105369818
0.925 0.040 12 68254842 upstream gene variant A/G snv 0.37 2
rs11935941
LOC107986195
1.000 0.040 4 148731326 intron variant A/C snv 0.31 2
rs1133076
TG
0.925 0.080 8 133113438 missense variant G/A snv 0.48 0.56 2
rs180223
TG
0.925 0.120 8 132888007 missense variant T/A;C;G snv 8.0E-06; 4.0E-06; 0.58 2
rs3753348
TNFRSF18
0.925 0.080 1 1208277 upstream gene variant C/G;T snv 2