Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1346512134 1.000 0.040 15 63042909 missense variant C/T snv 1
rs192883939 1.000 0.040 15 63057032 synonymous variant G/A snv 4.0E-06 7.0E-06 1
rs6738 1.000 0.040 15 63071702 3 prime UTR variant C/T snv 0.64 1
rs7178040 1.000 0.040 15 63071899 3 prime UTR variant G/T snv 0.13 1
rs886039024 1.000 0.040 15 63060900 missense variant A/G snv 1
rs74315379 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 6
rs727503512 0.851 0.080 1 201363349 missense variant G/A;C;T snv 4.0E-06 5
rs74315380 0.851 0.080 1 201364366 missense variant G/A;C snv 5
rs730881098 0.882 0.040 1 201365613 missense variant A/C snv 3
rs3729843 0.925 0.040 1 201367856 intron variant C/A;G;T snv 1.8E-04; 0.42 2
rs1892028 1.000 0.040 1 201367513 non coding transcript exon variant G/A snv 0.53 1
rs3729547 1.000 0.040 1 201365254 missense variant G/A;C snv 0.72 1
rs730881106 1.000 0.040 1 201362016 missense variant G/A snv 1
rs759758840 1.000 0.040 1 201365198 missense variant T/A;C snv 4.0E-06 1
rs778730615 1.000 0.040 1 201368194 missense variant G/A snv 1.2E-05 1.4E-05 1
rs984218824 1.000 0.040 1 201364324 missense variant C/T snv 4.0E-06 1
rs267607129 0.925 0.040 19 55151912 missense variant G/C snv 2
rs267607130 0.925 0.040 19 55157052 missense variant T/G snv 2
rs730881071 1.000 0.040 19 55154158 missense variant G/A snv 8.0E-06 2
rs1384750266 1.000 0.040 19 55154199 missense variant T/C snv 4.0E-06 1
rs267607124 0.807 0.080 3 52451410 missense variant G/A;C;T snv 4.0E-05; 4.0E-06; 1.3E-04 6
rs104893823 0.882 0.040 3 52451285 missense variant C/T snv 5
rs1471808574 1.000 0.040 3 52452128 missense variant C/T snv 7.0E-06 1
rs397516848 1.000 0.040 3 52451403 missense variant T/C snv 8.0E-06 1.4E-05 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169