Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs876657421
CBS
0.763 0.240 21 43063074 coding sequence variant -/CCCAGCAAAAGCCCCACCTGGATGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG;CCCAGCAAAAGCCCCACCTGGGTGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG delins 11
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs1395198370
VWF
12 6075370 missense variant A/G snv 7.0E-06 1
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs1056534 0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
rs753482 0.925 0.040 7 151009295 intron variant C/A;G;T snv 0.83; 4.0E-05; 3.1E-05; 4.4E-06 3
rs9818870 0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs1191926239 0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06 7
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs57920071 0.763 0.320 1 156136984 missense variant C/T snv 4.0E-06 7.0E-06 11
rs3848403 1.000 0.040 17 82736023 intron variant C/T snv 0.49 3
rs772155434 3 33058188 missense variant C/T snv 4.0E-06 1
rs910042982 2 11227257 missense variant C/T snv 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs11868035 0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs1050283 0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4
rs72551362 0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 4
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs754390004 1 100724804 missense variant T/A;C snv 1.2E-05 1
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21