Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146052672 0.851 0.160 6 34242693 intron variant -/C delins 5
rs1467568 0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1550805 0.925 0.120 5 68287979 intron variant C/T snv 6.9E-02 2
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs16861329 0.882 0.160 3 186948673 intron variant C/T snv 0.13 3
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs1799774 0.882 0.200 6 131882331 intron variant T/- delins 3
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs1968482 0.925 0.120 2 24863989 intron variant T/C snv 0.32 2
rs206936 0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs2072907 0.882 0.120 22 43936773 intron variant C/G snv 0.20 3
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2237895 0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs225011 0.925 0.120 14 80205865 intron variant T/A;C snv 2
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2302870 0.925 0.120 2 207088682 intron variant T/C;G snv 2
rs2568958 0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs290487 0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs361072 0.882 0.120 3 138759702 intron variant G/A;C snv 4