Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9