Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs851797 0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs3760396 0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15 13
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2494938 0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2180314 0.776 0.200 6 52752933 missense variant C/G snv 0.60 0.52 8