Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1046428 0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs11084033 0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691022 0.827 0.160 17 7670685 frameshift variant GG/A;G delins 6
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1136905 0.882 0.120 6 32518660 missense variant T/A;C snv 4.2E-03 3
rs113954997 0.882 0.280 11 14294844 missense variant T/A;C snv 3
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134