Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs114202211
HIPK1
0.827 0.120 1 113943285 intron variant T/C snv 8.1E-03 5
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 5
rs12075255
IL19
0.827 0.120 1 206788283 intron variant A/G snv 0.74 5
rs12131796
INAVA
0.827 0.120 1 200909599 intron variant G/A snv 0.22 5
rs183686347
IL23R
0.827 0.120 1 67237759 intron variant G/A snv 4.8E-03 5
rs2234161
TNFRSF14
0.827 0.120 1 2559766 non coding transcript exon variant C/T snv 4.1E-05; 0.55 0.58 5
rs3806308
RNF186
0.827 0.120 1 19816373 intron variant C/T snv 0.36 5
rs4655215 0.827 0.120 1 19811221 upstream gene variant T/C snv 0.68 5
rs4971079 0.827 0.120 1 155157915 intergenic variant G/A;C snv 5
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs6425143 0.827 0.120 1 172875212 intron variant T/G snv 0.34 5
rs6600247 0.827 0.120 1 24978623 intergenic variant T/C snv 0.55 5
rs6693105 0.827 0.120 1 152618187 downstream gene variant T/C snv 0.59 5
rs6697886 0.827 0.120 1 1238231 downstream gene variant G/A snv 0.21 5
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 5
rs78973538
GBAP1
0.827 0.120 1 155224224 intron variant C/T snv 4.8E-03 5
rs79568124 0.827 0.120 1 161533059 intron variant A/G snv 8.8E-02 5
rs80174646
IL23R
0.827 0.120 1 67242472 intron variant G/T snv 5.8E-02 5
rs1052571
CASP9
0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 4
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4