Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555454508 0.790 0.240 15 44615487 stop gained GTA/ATC mnv 18
rs312262717 0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 12
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800 0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs28456 0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs11829119 0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs141252918 0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17211233 0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs2054399 0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 4
rs9862857 0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs105633 0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs10744560 0.882 0.040 12 2277933 intron variant C/G;T snv 3
rs11125080 0.882 0.040 2 46505266 intron variant G/A;C snv 3
rs12052005 0.882 0.040 18 68832311 intron variant G/C;T snv 3
rs12149074 1.000 0.040 16 80071969 intron variant C/A;G snv 3
rs138449918 0.882 0.040 2 39936810 intron variant AT/-;ATAT delins 3
rs1906252 0.925 0.120 6 98102413 intron variant C/A;T snv 3