Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587778966 0.925 0.160 3 36996698 frameshift variant -/C delins 3
rs587778883 0.807 0.200 3 37025648 frameshift variant A/- del 6
rs587778914 0.925 0.160 3 36996645 missense variant A/C snv 2
rs63750710 0.925 0.160 3 37020411 missense variant A/C snv 1
rs35045067 0.925 0.160 3 37048557 missense variant A/C;G snv 4.4E-05 1
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs267607906 1.000 0.160 3 37050576 stop gained A/C;G;T snv 1
rs587778964 0.882 0.160 3 37048604 missense variant A/C;T snv 1
rs63750511 0.925 0.160 3 37040252 missense variant A/C;T snv 1
rs1260021106 0.925 0.160 3 37025645 missense variant A/G snv 1.6E-05 2
rs1392665848 0.925 0.160 3 37025865 missense variant A/G snv 4.0E-06 2
rs63750211 0.882 0.160 3 37008904 missense variant A/G snv 2
rs41295282 1.000 0.160 3 37001024 missense variant A/G snv 1.6E-05 7.0E-05 1
rs786201226 0.925 0.160 3 37014450 synonymous variant A/G;T snv 4.0E-06 2
rs63751094 0.925 0.160 3 36996624 stop lost A/G;T snv 1
rs35502531 0.827 0.160 3 37047639 missense variant AA/GC mnv 7
rs63750339 0.925 0.200 3 37020441 frameshift variant C/- delins 3
rs63749818 0.925 0.160 3 37007002 stop gained C/A;G;T snv 2
rs63750114 0.827 0.160 3 37049015 stop gained C/A;T snv 4.9E-04 4
rs63751194 0.851 0.160 3 37017508 missense variant C/A;T snv 4.0E-06 3
rs63751428 0.882 0.160 3 36996686 stop gained C/A;T snv 1
rs63751615 0.851 0.200 3 37012098 stop gained C/A;T snv 4.0E-06 1
rs1418586322 0.827 0.160 3 37050495 missense variant C/G snv 4.0E-06 6
rs63750899 0.851 0.200 3 37048562 missense variant C/G;T snv 4
rs63750781 0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 1