Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10758593 0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs11154178 0.807 0.240 6 123540174 intron variant T/A;C snv 7
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2260000 0.851 0.200 6 31625699 intron variant A/G snv 0.29 7
rs28485846 0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02 7
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs6910071 0.790 0.320 6 32315077 intron variant A/G snv 0.14 7
rs71597855 0.807 0.240 4 53790270 intron variant G/A snv 2.5E-02 7
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs80028505 0.807 0.240 6 36030611 intron variant C/G;T snv 7
rs910049 0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22