Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs10553577
STAT4
1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 1
rs11048434
KLRG1
1.000 0.200 12 9001336 intron variant G/A snv 0.28 1
rs115575857 1.000 0.200 6 32691868 regulatory region variant A/G snv 1
rs1507153 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 1
rs17074492
LOC105370283
1.000 0.200 13 81587764 intergenic variant C/A;T snv 1
rs17339836
TNPO3
1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 1
rs1957173 1.000 0.200 14 45937713 intron variant C/T snv 4.6E-02 1
rs6579837
TNIP1
1.000 0.200 5 151055333 intron variant G/T snv 0.11 1
rs7119038 1.000 0.200 11 118867572 intergenic variant G/A snv 0.77 1
rs7999279 1.000 0.200 13 47376590 intergenic variant A/C snv 0.76 1
rs9271573 1.000 0.200 6 32622724 TF binding site variant A/C snv 0.55 1
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs9938751
SHISA9
1.000 0.200 16 12908502 missense variant T/A;C snv 0.88 1