Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs340874 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs17712208 1 213977102 intron variant T/A snv 2.1E-02 2
rs340878 1 213983706 intron variant G/C snv 0.63 2
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs13404446 0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs2305929 1.000 0.040 2 27891044 intron variant A/G snv 0.14 4
rs4665965 0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs780110 0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
rs853789 2 168944978 intron variant A/G;T snv 0.75 4
rs1371614 2 26930006 intron variant C/T snv 0.29 3
rs1124649 2 27037601 missense variant G/A snv 0.32 0.35 2
rs11891554 2 27390750 intron variant G/A;T snv 7.1E-02 2
rs2390732 2 168749457 intron variant G/A snv 0.65 2
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs11920090 1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs7651090 0.925 0.080 3 185795604 intron variant A/G snv 0.39 5
rs2877716 3 123375604 intron variant T/C snv 0.76 4
rs11717195 1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs1280 3 170995501 intron variant T/C snv 0.20 2