Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10