Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205