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
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
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
rs174550 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs7607980 1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8