Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60