Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115559990 6 29926633 non coding transcript exon variant C/G;T snv 1
rs2523946 0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv 1
rs3823355 1.000 0.040 6 29974306 upstream gene variant C/A;T snv 1
rs6914699 6 29966245 downstream gene variant T/C snv 0.41 1
rs2523933 6 29964515 intergenic variant G/C;T snv 1
rs2571400 6 29959945 downstream gene variant C/G snv 0.51 1
rs3893463 6 29967628 downstream gene variant C/T snv 0.41 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
rs2975009 6 29930339 upstream gene variant C/T snv 0.50 1
rs1061539 1.000 0.040 6 29969778 downstream gene variant T/A;C 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
rs17882753 6 29944817 non coding transcript exon variant C/T snv 1.4E-02 1
rs115729734 1.000 0.080 6 29931238 upstream gene variant T/C;G snv 1
rs16896742 6 29954963 upstream gene variant A/G snv 0.35 1
rs28749114 6 29937675 upstream gene variant A/G;T snv 1
rs114577328 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 1
rs9259819 6 29925798 upstream gene variant G/T snv 0.49 1
rs2394250 1.000 0.040 6 29975879 intron variant G/T snv 0.40 1
rs3132685 0.807 0.320 6 29978172 intron variant G/A;T snv 1
rs2517873 1.000 0.080 6 29908215 intron variant G/A snv 0.15 1
rs115928623 1.000 0.080 6 29971371 intron variant A/T snv 1