Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213