Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41292470
LOC285626
0.925 0.200 5 159333192 intron variant TTAGAG/GC delins 3
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs146054764
CASP9
0.882 0.160 1 15506000 missense variant T/G snv 1.4E-03; 8.0E-06 1.4E-03 4
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 4
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs6726160
NONOP2
1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 3
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs1223438908
CBLB
1.000 0.120 3 105681480 missense variant T/G snv 4.0E-06 2
rs1252641479
ARHGEF7
1.000 0.040 13 111300800 missense variant T/G snv 4.0E-06 2
rs752455542
CBLB
1.000 0.120 3 105681740 missense variant T/G snv 4.0E-06 2
rs786204847
DDX58
1.000 9 32488039 missense variant T/G snv 2
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs1517440
LOC105373895
1.000 0.080 2 220589153 intron variant T/C;G snv 2
rs1052237
NUS1
6 117694118 stop gained T/C;G snv 8.8E-05 8.4E-05 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25