Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 40
rs10088218 0.851 0.120 8 128531703 intron variant G/A snv 0.13 3
rs10098821 0.882 0.120 8 128546982 intron variant C/T snv 7.6E-02 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
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 43
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
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
rs1057519865 0.742 0.240 3 138946321 missense variant G/C snv 15
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 213
rs1131691022 0.827 0.160 17 7670685 frameshift variant GG/A;G delins 4
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs1136905 0.882 0.120 6 32518660 missense variant T/A;C snv 4.2E-03 3
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 31