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 53
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
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
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1467465 0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs1469713 0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs200182588 0.827 0.160 9 104094409 5 prime UTR variant -/GC ins 7.0E-06 6
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16