Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4313034 0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78 2
rs2571400 6 29959945 downstream gene variant C/G snv 0.51 1
rs2975009 6 29930339 upstream gene variant C/T snv 0.50 1
rs9259819 6 29925798 upstream gene variant G/T snv 0.49 1
rs3893464 1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46 3
rs9260313 6 29949108 downstream gene variant T/C snv 0.42 2
rs6914699 6 29966245 downstream gene variant T/C snv 0.41 1
rs3893463 6 29967628 downstream gene variant C/T snv 0.41 1
rs2394250 1.000 0.040 6 29975879 intron variant G/T snv 0.40 1
rs16896742 6 29954963 upstream gene variant A/G snv 0.35 1
rs60131261 1.000 0.040 6 29969559 downstream gene variant TTTA/- delins 0.26 1
rs9260620 6 29955314 upstream gene variant T/G snv 0.24 7
rs2524005 0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 2
rs7758512 1.000 6 30002812 intron variant T/G snv 0.17 4
rs2523961 0.925 0.120 6 29971803 non coding transcript exon variant G/A snv 0.16 2
rs2517873 1.000 0.080 6 29908215 intron variant G/A snv 0.15 1
rs9260151 1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14 2
rs3094146 1.000 0.080 6 30003183 non coding transcript exon variant G/C snv 6.1E-02 1
rs192543598 6 29963568 downstream gene variant A/G snv 1.6E-02 2
rs17882753 6 29944817 non coding transcript exon variant C/T snv 1.4E-02 1
rs7749944 0.925 6 29992223 upstream gene variant A/C snv 1.3E-02 2
rs114577328 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 1
rs114204022 1.000 0.040 6 29972902 upstream gene variant G/A snv 2
rs113205291 1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs115625073 1.000 0.040 6 29924456 upstream gene variant T/C snv 2