Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs11651052 0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs11671664 0.925 0.120 19 45669020 intron variant G/A snv 0.12 4
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs11709077 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs1470579 0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs1899951 0.851 0.160 3 12353341 intron variant C/T snv 0.26 2
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 4
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 5
rs2237897 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 3
rs2246012 1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs2299383 1.000 0.080 7 103778399 intron variant C/T snv 0.41 2
rs329122 1.000 0.080 5 134528909 intron variant G/A snv 0.45 2
rs35261542 1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 7
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs4865796 1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs6947395 1.000 0.080 7 69941675 intron variant A/T snv 0.20 2
rs7034200 1.000 0.080 9 4289050 intron variant C/A;G snv 3