Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs6700896 0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs3772622 0.851 0.080 3 148717966 intron variant T/A;C snv 4