Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs301806 0.851 0.120 1 8422018 intron variant C/T snv 0.62 6
rs10462028 0.882 0.120 4 55432133 3 prime UTR variant G/A snv 0.28 4
rs34668726 1.000 0.040 2 23673031 intron variant C/G snv 0.13 3