Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104