Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1448674651 0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12