Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs10814916 0.851 0.200 9 4293150 intron variant A/C snv 0.57 7