Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10484566 0.925 0.200 6 32867481 regulatory region variant T/G snv 6.8E-02 2
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 2
rs1214611 0.925 0.200 1 167479867 intron variant A/G snv 0.54 2
rs12177980 0.925 0.200 6 32718307 non coding transcript exon variant G/A snv 0.37 2
rs154981 0.925 0.200 6 32913216 regulatory region variant C/A;G;T snv 2
rs2027856 0.925 0.200 6 32434928 upstream gene variant G/A snv 0.18 2
rs2050189 0.925 0.200 6 32371870 5 prime UTR variant T/C;G snv 0.18 2
rs206015 0.925 0.200 6 32214982 intron variant G/A snv 0.15 2
rs2064478 0.925 0.200 6 33104489 intron variant C/T snv 0.28 2
rs2071540 0.925 0.200 6 32845139 non coding transcript exon variant T/C snv 0.61 2
rs2071554 0.925 0.200 6 32816899 missense variant C/A;T snv 4.1E-06; 6.2E-02 2
rs2076537 0.925 0.200 6 32349858 non coding transcript exon variant G/A snv 0.37 0.42 2
rs2256965 0.925 0.200 6 31587353 non coding transcript exon variant A/G;T snv 0.60 2
rs2267644 0.925 0.200 6 32224783 upstream gene variant G/A snv 4.9E-02 2
rs2280800 0.925 0.200 6 31678621 intron variant C/A snv 0.14 2
rs2395150 0.925 0.200 6 32358268 intron variant G/A snv 0.51 2
rs2395162 0.925 0.200 6 32420003 intergenic variant G/T snv 0.13 2
rs2395175 0.925 0.200 6 32437249 upstream gene variant G/A snv 0.12 2
rs241407 0.925 0.200 6 32894963 upstream gene variant C/T snv 9.7E-02 2
rs241409 0.925 0.200 6 32894143 upstream gene variant A/G snv 9.8E-02 2
rs241424 0.925 0.200 6 32837157 intron variant G/A snv 0.50 2
rs2516440 0.925 0.200 6 31472720 intron variant G/A snv 0.41 2
rs2844533 0.925 0.200 6 31383025 upstream gene variant G/A snv 0.74 2
rs2844746 0.925 0.200 6 30371825 intergenic variant T/C snv 0.69 2
rs3129962 0.925 0.200 6 32411606 upstream gene variant G/A;C snv 2