Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2072446 0.776 0.160 17 49510457 missense variant C/T snv 5.2E-02 4.1E-02 11
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72