Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98