Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2285932 0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 5
rs669260 0.851 0.080 9 32503442 intron variant T/A;C snv 4
rs5745568 0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs6141 0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs750898115 0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 4
rs1805016 0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 3
rs1131454 0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs1285933 0.925 0.040 7 141927349 intron variant G/A snv 0.54 2
rs3205166 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 2
rs1447043692 0.925 0.040 10 98641918 missense variant C/T snv 2
rs3739319 0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 2
rs371057322 0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs4859584 1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 1
rs15895 1.000 0.040 12 113010483 stop lost A/G;T snv 0.75 1