Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs7133378 12 123924955 intron variant G/A snv 0.38 6
rs62104180 2 466003 intergenic variant G/A snv 2.9E-02 4
rs6545714 2 59080590 intron variant G/A;C snv 4
rs6755502 2 635721 intergenic variant T/C snv 0.85 3