Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs4143094
GATA3
0.752 0.240 10 8047173 intron variant T/G snv 0.70 12
rs2073440
HDC
0.851 0.200 15 50242317 missense variant T/G snv 3.4E-02 5.9E-02 4
rs7328203
LINC02341
1.000 0.120 13 42414410 intron variant T/G snv 0.48 2
rs11027293 1.000 0.120 11 23530907 intergenic variant T/G snv 2.4E-02 1
rs2606618 1.000 0.120 6 122095195 intergenic variant T/G snv 0.19 1
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs6692977
FCRL5
0.882 0.200 1 157517598 intron variant T/C;G snv 3
rs257174
LOC101929524
1.000 0.120 5 16628402 intron variant T/C;G snv 1
rs2780815
JAK1
1.000 0.120 1 64835928 intron variant T/C;G snv 1
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs1135216
PSMB9 ; TAP1
0.807 0.200 6 32847198 missense variant T/C snv 0.17 0.18 6
rs9494885
LOC107986649 ; WAKMAR2
0.882 0.320 6 137851611 intron variant T/C snv 0.20 3
rs11677002
FOSL2 ; FLJ31356
1.000 0.120 2 28391534 intron variant T/C snv 0.39 1
rs12939457
ZPBP2
1.000 0.120 17 39875935 intron variant T/C snv 0.38 1
rs1373976132
HNMT
1.000 0.120 2 137964586 missense variant T/C snv 4.0E-06 1