Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18