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
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23