Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13063604 0.882 0.120 3 128085887 intron variant G/A snv 0.23 3
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1444192401 0.882 0.120 12 52235347 missense variant G/A snv 4
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
rs1516982 0.882 0.120 8 128521400 intron variant A/G snv 0.16 3
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
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
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1801200 0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs1836724 0.807 0.240 2 211380227 3 prime UTR variant G/A snv 0.57 6
rs185229225 0.851 0.120 4 13607505 intron variant T/C snv 4
rs186724 0.882 0.120 1 110018293 intron variant C/G;T snv 3
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
rs2072590 0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 4
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs2191249 0.882 0.120 17 61758503 intron variant T/G snv 0.79 3
rs2287497 0.882 0.120 17 7689462 intron variant G/A snv 0.25 3
rs2297235 0.752 0.320 10 104274733 5 prime UTR variant A/G snv 0.22 11