Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs1178979 0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21 6
rs17145713 0.925 0.120 7 73490480 intron variant C/T snv 0.21 6
rs1919127 0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 6
rs1919128 0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs3749147 0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs13022873 0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs4666002 0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs11983997 0.925 0.120 7 73524914 upstream gene variant G/A;C snv 5
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 5
rs1178977 0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 5
rs6976930 0.925 0.120 7 73471480 intron variant G/A snv 0.23 5
rs7811265 0.925 0.120 7 73520180 intron variant A/G snv 0.23 5
rs10208529 0.925 0.120 2 27563321 intron variant A/T snv 0.28 5
rs4665382 0.925 0.120 2 27560934 intron variant T/C snv 0.23 5
rs4665383 0.925 0.120 2 27568688 synonymous variant C/G snv 0.24 5
rs4665991 0.925 0.120 2 27543417 intron variant G/A snv 0.24 5
rs13002853 0.925 0.120 2 27630378 intron variant C/G snv 0.20 5
rs867186 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 5
rs12467476 0.925 0.120 2 27602848 intron variant T/C snv 0.23 5