Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17074492
LOC105370283
1.000 0.200 13 81587764 intergenic variant C/A;T snv 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
rs115575857 1.000 0.200 6 32691868 regulatory region variant A/G snv 1
rs1085308048
PTEN
0.851 0.320 10 87933175 stop gained T/G snv 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs9938751
SHISA9
1.000 0.200 16 12908502 missense variant T/A;C snv 0.88 1
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs9271573 1.000 0.200 6 32622724 TF binding site variant A/C snv 0.55 1
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 6