Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2300747 0.882 0.200 1 116561593 intron variant A/G snv 0.19 3
rs12044852 0.925 0.120 1 116545157 intron variant C/A snv 0.12 2
rs1335532 1.000 0.080 1 116558335 intron variant A/G snv 0.28 1
rs6677309 1.000 0.080 1 116537544 intron variant A/C snv 0.28 1
rs1414273 1.000 0.080 1 116560027 non coding transcript exon variant C/T snv 0.15 0.27 1