Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111401431 0.763 0.200 15 48468097 missense variant G/A snv 2
rs137854464 0.851 0.200 15 48425483 missense variant C/T snv 7.0E-06 2
rs137854480 0.742 0.200 15 48537629 missense variant G/A snv 2
rs111588631 1.000 0.160 15 48428391 missense variant A/G snv 1
rs111929350 1.000 0.160 15 48452603 missense variant C/A;G;T snv 1
rs111984349 0.763 0.200 15 48415759 missense variant C/T snv 1
rs112375043 0.925 0.160 15 48472594 stop gained G/A;C;T snv 3.6E-05 1.4E-05 1
rs112660651 0.925 0.160 15 48610808 missense variant C/A;G;T snv 1
rs112728248 0.925 0.160 15 48448812 missense variant C/T snv 1
rs112836174 0.925 0.160 15 48430791 missense variant A/G;T snv 1
rs113544411 0.925 0.160 15 48421652 stop gained G/A;C;T snv 1.2E-05 1
rs137854456 0.925 0.160 15 48487365 missense variant C/A;G;T snv 4.0E-06; 4.0E-05 1
rs137854457 0.925 0.160 15 48428423 missense variant C/G;T snv 1
rs137854458 1.000 0.160 15 48483910 missense variant C/G snv 1
rs137854459 1.000 0.160 15 48463977 missense variant A/G snv 1
rs137854460 0.925 0.160 15 48432943 missense variant C/G;T snv 1
rs137854461 0.790 0.280 15 48437026 missense variant T/C snv 1
rs137854462 1.000 0.160 15 48510115 missense variant T/A snv 1
rs137854463 1.000 0.160 15 48497391 missense variant T/G snv 1
rs137854465 0.925 0.160 15 48488230 missense variant A/G snv 1
rs137854467 0.790 0.280 15 48600217 missense variant G/A snv 1
rs137854468 0.851 0.160 15 48487396 missense variant C/T snv 1
rs137854469 1.000 0.160 15 48485418 missense variant C/A;T snv 1
rs137854470 1.000 0.160 15 48487425 missense variant C/T snv 1
rs137854471 0.925 0.160 15 48483931 missense variant C/T snv 1