Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10050860
ERAP1
0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 4
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 6
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs10236188 1.000 0.200 7 150548168 intergenic variant T/C snv 0.49 1
rs10256482 1.000 0.200 7 150653887 intergenic variant T/C snv 0.47 1
rs10277380 1.000 0.200 7 150533604 intergenic variant T/A;C snv 1
rs10454134 1.000 0.200 2 48420887 TF binding site variant G/A snv 0.14 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs104894559
CA4
0.882 0.200 17 60150074 missense variant C/T snv 2.5E-04 1.4E-04 3
rs104895083
MEFV
0.925 0.200 16 3247166 missense variant G/C;T snv 4.0E-05; 1.2E-05 2
rs104895094
MEFV
0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs104895297
MVK
0.882 0.360 12 109581427 missense variant C/T snv 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs10515746
HAVCR2
0.925 0.240 5 157109557 intron variant A/C;T snv 2
rs1057519328
MEFV
1.000 0.200 16 3249592 missense variant G/C snv 2.1E-05 1
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1065407
ERAP1 ; CAST ; LOC102724748
1.000 0.200 5 96776379 3 prime UTR variant T/A;G snv 3.3E-05; 0.26 1
rs10863888
TRAF5
0.851 0.280 1 211329427 intron variant A/C;G;T snv 4
rs111874856
ROCK1
1.000 0.200 18 21028924 missense variant C/T snv 1
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs112108028
ROCK1
1.000 0.200 18 20959861 missense variant G/A snv 1
rs112130712
ROCK1
1.000 0.200 18 20967783 missense variant T/C snv 1
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8