Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs11205303 0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs7133378 12 123924955 intron variant G/A snv 0.38 6
rs10968577 9 28415514 intron variant C/T snv 0.27 3
rs757318 19 18709498 intron variant C/A;G;T snv 3