Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs9610 0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs872071 0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs80202369 1.000 0.120 11 118873150 intergenic variant G/A snv 6.6E-03 1
rs799917 0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs78440425 1.000 0.120 11 118888302 intron variant G/A snv 1.1E-02 1
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs766588452 1.000 0.120 1 65621389 missense variant A/C;G snv 8.0E-06; 2.0E-05 1
rs764168570 1.000 0.120 3 12608879 synonymous variant C/T snv 7.0E-06 1
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs758837678 0.925 0.120 8 90001503 missense variant C/T snv 2
rs758835365
FAS
1.000 0.120 10 89010795 stop gained C/T snv 8.0E-06 7.0E-06 1
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs754651345 1.000 0.120 5 159326751 missense variant A/G snv 4.0E-06 1
rs75002266 0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28