Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs11558471 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs340874 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs1470579 0.925 0.160 3 185811292 intron variant A/C snv 0.46 3
rs7173964 1.000 0.080 15 62104743 regulatory region variant G/A snv 0.49 2