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
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1571801 0.827 0.120 9 121665094 intron variant G/T snv 0.21 6
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs17021918 0.776 0.240 4 94641726 intron variant C/T snv 0.30 8
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs2242652 0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs28360317 0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs3750861 0.827 0.120 10 3782241 intron variant C/T snv 8.2E-02 6.6E-02 5
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs7726159 0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs8102476 0.776 0.240 19 38244973 intron variant C/T snv 0.40 8