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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
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
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 9
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs2077647 0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs975263 0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7