Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2517713 1.000 0.120 6 29950322 downstream gene variant G/A;T snv 1
rs3132685 0.807 0.320 6 29978172 intron variant G/A;T snv 1
rs3094146 1.000 0.080 6 30003183 non coding transcript exon variant G/C snv 6.1E-02 1
rs114577328 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 1
rs2523933 6 29964515 intergenic variant G/C;T snv 1
rs2394250 1.000 0.040 6 29975879 intron variant G/T snv 0.40 1
rs9259819 6 29925798 upstream gene variant G/T snv 0.49 1
rs1061539 1.000 0.040 6 29969778 downstream gene variant T/A;C snv 1
rs9260489 1.000 0.080 6 29952555 upstream gene variant T/A;G snv 2
rs115625073 1.000 0.040 6 29924456 upstream gene variant T/C snv 2
rs144304366 1.000 0.040 6 29936216 downstream gene variant T/C snv 2
rs9260313 6 29949108 downstream gene variant T/C snv 0.42 2
rs6914699 6 29966245 downstream gene variant T/C snv 0.41 1
rs150881176 1.000 0.120 6 29979963 downstream gene variant T/C snv 1
rs115729734 1.000 0.080 6 29931238 upstream gene variant T/C;G snv 1
rs9260620 6 29955314 upstream gene variant T/G snv 0.24 7
rs7758512 1.000 6 30002812 intron variant T/G snv 0.17 4
rs111312615 1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs60131261 1.000 0.040 6 29969559 downstream gene variant TTTA/- delins 0.26 1