Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1033182 0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10951982 0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11089788 0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs12431381 0.925 0.080 14 59643053 intron variant T/C snv 0.35 2
rs12434215 0.882 0.160 14 59642862 intron variant A/G snv 0.33 3
rs12437854 0.925 0.080 15 93598604 intron variant T/G snv 0.10 2
rs12917114 0.925 0.080 15 47852953 intron variant C/T snv 8.9E-02 2
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1516792 0.925 0.080 2 112778356 intron variant G/A snv 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs161740 0.882 0.200 5 98869326 intron variant C/A;T snv 3
rs1709183 0.882 0.160 6 151872861 intron variant C/T snv 0.67 3
rs17173608 0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs1749824 0.925 0.080 10 79164105 intron variant C/A snv 0.39 3
rs17709344 0.925 0.080 15 93608310 intron variant G/A snv 4.0E-02 2
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs183962941 0.925 0.080 16 20343125 intron variant G/A snv 1.1E-02 2
rs1952034 0.882 0.160 14 59691018 intron variant C/T snv 0.35 3
rs2032487 0.882 0.080 22 36299382 intron variant C/T snv 0.78 3
rs2232365 0.716 0.480 X 49259429 intron variant T/C snv 16
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2294021 0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs2413396 0.925 0.080 22 36312039 intron variant C/G;T snv 0.88 2