Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs174570 0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11