Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs2657879 1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs4481233 0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs7200543 16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 4