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
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46