Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs200100285 0.851 0.080 1 11796313 missense variant T/C;G snv 1.9E-04 4
rs121434296 0.882 0.040 1 11794766 missense variant G/A snv 2.0E-05 3.5E-05 3
rs760161369 0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 3
rs786204030 0.882 0.080 1 11791276 stop gained C/T snv 3
rs121434295 0.925 1 11801166 missense variant C/T snv 3.6E-05 2.1E-05 2
rs121434297 0.925 1 11795161 missense variant A/G snv 1.2E-05 7.0E-06 2
rs147257424 0.925 0.080 1 11801299 missense variant C/A;G;T snv 1.2E-05; 1.2E-05 2
rs267606886 0.925 1 11795114 missense variant A/C snv 2
rs267606887 0.925 1 11795158 missense variant T/C snv 2
rs754980119 0.925 0.280 1 11802962 missense variant C/G;T snv 4.0E-06; 5.6E-05 2
rs1057519359 1.000 1 11802880 splice donor variant C/T snv 1
rs1057519360 1.000 1 11801220 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1057519361 1.000 1 11796382 missense variant G/T snv 1
rs1057519362 1.000 1 11796324 frameshift variant C/- delins 1
rs1057519363 1.000 1 11792317 frameshift variant C/- del 1
rs1182635980 1.000 1 11800275 missense variant C/T snv 1
rs138189536 1.000 1 11802981 missense variant G/A snv 2.0E-04 7.7E-05 1
rs1430872491 1.000 1 11794735 missense variant C/T snv 8.0E-06 7.0E-06 1
rs144508139 1.000 1 11791244 missense variant G/A snv 1.6E-05 1
rs1553187509 1.000 1 11801399 missense variant C/A snv 1
rs1553188112 1.000 1 11803156 5 prime UTR variant AG/- del 1
rs1557761665 1.000 1 11794437 frameshift variant -/C delins 1