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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 27
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 19