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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19