Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2523933 6 29964515 intergenic variant G/C;T snv 1
rs6914699 6 29966245 downstream gene variant T/C snv 0.41 1
rs3893464 1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46 3
rs3893463 6 29967628 downstream gene variant C/T snv 0.41 1
rs60131261 1.000 0.040 6 29969559 downstream gene variant TTTA/- delins 0.26 1
rs1061539 1.000 0.040 6 29969778 downstream gene variant T/A;C snv 1
rs115928623 1.000 0.080 6 29971371 intron variant A/T snv 1
rs2523961 0.925 0.120 6 29971803 non coding transcript exon variant G/A snv 0.16 2
rs114204022 1.000 0.040 6 29972902 upstream gene variant G/A snv 2
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
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
rs150881176 1.000 0.120 6 29979963 downstream gene variant T/C snv 1
rs114950038 1.000 0.040 6 29983056 downstream gene variant G/A;C snv 2
rs7749944 0.925 6 29992223 upstream gene variant A/C snv 1.3E-02 2
rs7758512 1.000 6 30002812 intron variant T/G snv 0.17 4
rs3094146 1.000 0.080 6 30003183 non coding transcript exon variant G/C snv 6.1E-02 1
rs4313034 0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78 2