Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228479 0.763 0.280 16 89919532 missense variant G/A;C snv 7.8E-02; 4.0E-06 11
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs2308327 0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 10
rs735665 0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs1494555 0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs3763313 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs3212961 0.827 0.200 19 45419065 intron variant G/A;T snv 1.9E-04; 0.20 7
rs3020314 0.790 0.280 6 151949537 intron variant C/G;T snv 7
rs1308699981 0.807 0.440 1 161543085 missense variant G/A snv 4.0E-06 7
rs12711521 0.807 0.240 1 11030859 missense variant C/A snv 0.74 0.63 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs1392080411 0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06 5
rs4937362 0.827 0.240 11 128622844 intron variant T/C snv 0.49 5
rs12355840 0.827 0.240 10 133247608 non coding transcript exon variant C/G;T snv 1.1E-04; 0.80 5
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4
rs4938573 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 4
rs10190751 0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4
rs13254990 0.882 0.120 8 128064205 intron variant C/T snv 0.24 4
rs1056503 0.851 0.200 5 83353158 synonymous variant T/A;G snv 4.0E-06; 0.23 4
rs3115667 0.882 0.200 6 31675622 downstream gene variant T/A;C snv 0.74 3
rs2857597 0.882 0.200 6 31617223 upstream gene variant T/A snv 0.74 3
rs3117222 0.882 0.280 6 33093172 intron variant C/T snv 0.33 3