Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918416 0.882 0.160 5 151851440 missense variant C/T snv 4
rs121918413 1.000 0.120 5 151851470 missense variant G/T snv 3
rs762864856 0.925 0.200 5 151856384 splice acceptor variant C/G;T snv 8.0E-06 3
rs121918410 1.000 0.120 5 151829060 missense variant T/C;G snv 4.0E-06 2
rs281864919 1.000 0.120 5 151822764 missense variant C/T snv 4.8E-05 2
rs281864921 1.000 0.120 5 151829059 frameshift variant A/- del 2
rs121918408 1.000 0.120 5 151851406 missense variant C/A;T snv 2
rs121918409 1.000 0.120 5 151851487 missense variant A/T snv 2
rs121918415 1.000 0.120 5 151855047 stop gained G/A;T snv 2
rs121918417 1.000 0.120 5 151851525 missense variant G/C snv 2
rs121918411 1.000 0.120 5 151851420 missense variant C/A;G snv 2
rs121918412 1.000 0.120 5 151851392 missense variant T/C snv 2
rs267606848 1.000 0.120 5 151851418 missense variant C/T snv 2
rs1181626947 1.000 0.120 5 151822777 missense variant C/T snv 4.0E-06 1
rs121918418 1.000 0.120 5 151829009 stop gained G/T snv 1.4E-05 1
rs281864913 1.000 0.120 5 151828950 stop gained G/A snv 4.8E-05 2.1E-05 1
rs1554083576 1.000 0.120 5 151851443 missense variant T/C snv 1
rs1554085893 1.000 0.120 5 151886719 splice donor variant A/G snv 1
rs199547699 1.000 0.120 5 151859984 missense variant G/A;T snv 1.2E-05; 4.0E-06 1
rs281864918 1.000 0.120 5 151851463 missense variant C/T snv 2.4E-05 7.0E-06 1
rs121918414 1.000 0.120 5 151856337 missense variant T/C snv 4.0E-06 1.4E-05 1
rs281864915 1.000 0.120 5 151859963 frameshift variant G/- delins 2.8E-05 1
rs751659671 1.000 0.120 5 151851566 missense variant G/A snv 1.6E-05 1