Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs7970350 12 65966384 downstream gene variant C/T snv 0.48 4
rs8010717 14 79944098 intron variant T/C snv 0.29 4
rs4947642 7 51797912 intergenic variant A/C;G snv 3
rs7889 6 31637671 3 prime UTR variant C/G snv 0.58 2