Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs8040868 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs2869967 0.827 0.120 4 88948181 intron variant T/C snv 0.49 11
rs17486278 0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs12504628 1.000 0.040 4 144515172 intron variant T/C snv 0.33 6
rs1980057 1.000 0.040 4 144564586 intron variant C/T snv 0.31 6
rs13147758 4 144539078 intron variant A/G snv 0.31 5
rs8031948 1.000 0.040 15 78523715 intron variant G/T snv 0.27 5