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
rs132774 0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs390802 0.827 0.160 3 52397655 intron variant G/A snv 0.16 5
rs5751129 0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
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
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057520001 0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs12163565 0.827 0.160 3 52396510 missense variant G/A snv 0.19 0.16 5
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79