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
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
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
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs181206 0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 16
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 20