Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs398122965 0.807 0.280 16 2496872 missense variant C/T snv 1.2E-05 2.8E-05 13
rs398122967 0.827 0.280 16 2498262 frameshift variant T/- del 7.4E-05 4.9E-05 12
rs201257588 0.882 0.280 16 2496206 stop gained C/G;T snv 6.0E-05 9
rs398122966 0.882 0.280 16 2496266 missense variant C/T snv 8.0E-06 9
rs398122968 0.882 0.280 16 2499425 splice region variant G/A snv 9
rs747821285 0.882 0.280 16 2496476 missense variant G/A snv 4.1E-06 9
rs760474458 0.882 0.280 16 2496267 missense variant G/A;C;T snv 4.0E-06; 2.0E-05; 4.0E-06 9
rs797044548 0.882 0.280 16 2498253 missense variant G/T snv 9
rs376712059 0.827 0.280 16 2496605 stop gained G/A;C;T snv 6.9E-05; 8.1E-06; 4.1E-06 5
rs765965968 0.882 0.080 16 2498333 missense variant G/A;T snv 1.3E-05; 4.2E-06 5
rs1057524191 0.925 0.040 16 2496269 stop gained C/T snv 3
rs1555501140 0.925 0.040 16 2496319 frameshift variant C/- delins 3
rs1567413218 0.925 0.040 16 2498385 stop gained C/G snv 3
rs483352866 0.882 0.240 16 2496681 missense variant C/G;T snv 8.0E-06 3
rs747538224 0.925 0.040 16 2496993 missense variant C/G snv 1.8E-04 2.1E-05 3
rs1567411469 0.925 16 2496494 stop gained A/T snv 2
rs1057519629 16 2498332 missense variant C/G;T snv 2.1E-05 1
rs1335526524 1.000 0.080 16 2498249 missense variant A/G snv 7.0E-06 1
rs1555501320 1.000 16 2497067 missense variant A/C snv 1
rs199700840 1.000 16 2497026 missense variant G/A;C snv 1.9E-04; 8.0E-06 1
rs202162520 1.000 0.040 16 2496317 missense variant C/A;T snv 4.0E-06; 1.9E-03 1
rs267607103 1.000 0.040 16 2496587 missense variant G/A;C snv 1.3E-04; 4.1E-06 1
rs267607104 1.000 0.040 16 2496899 missense variant T/C snv 1
rs267607105 1.000 0.040 16 2500822 missense variant C/T snv 8.3E-06 2.1E-05 1
rs397514713 1.000 16 2496834 missense variant T/C snv 1