Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111312615 1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs144304366 1.000 0.040 6 29936216 downstream gene variant T/C snv 2
rs114950038 1.000 0.040 6 29983056 downstream gene variant G/A;C snv 2
rs9260151 1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14 2
rs9260489 1.000 0.080 6 29952555 upstream gene variant T/A;G snv 2
rs115928623 1.000 0.080 6 29971371 intron variant A/T snv 1
rs2517873 1.000 0.080 6 29908215 intron variant G/A snv 0.15 1
rs150881176 1.000 0.120 6 29979963 downstream gene variant T/C snv 1
rs2860580 1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv 1
rs2517713 1.000 0.120 6 29950322 downstream gene variant G/A;T snv 1
rs2394250 1.000 0.040 6 29975879 intron variant G/T snv 0.40 1
rs1061539 1.000 0.040 6 29969778 downstream gene variant T/A;C snv 1
rs3823355 1.000 0.040 6 29974306 upstream gene variant C/A;T snv 1
rs60131261 1.000 0.040 6 29969559 downstream gene variant TTTA/- delins 0.26 1
rs41546314 1.000 0.040 6 29942601 synonymous variant C/T snv 0.26 1
rs147097402 1.000 0.080 6 29930083 upstream gene variant C/A;G;T snv 1
rs3094146 1.000 0.080 6 30003183 non coding transcript exon variant G/C snv 6.1E-02 1
rs115729734 1.000 0.080 6 29931238 upstream gene variant T/C;G snv 1
rs114577328 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 1