Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34332679 14 35412760 regulatory region variant -/A;AA delins 2
rs3831732 10 87895485 intron variant -/A;AA delins 2
rs58548501 4 54635119 intergenic variant -/A;ATTTTTTTTTA ins 0.43 4
rs145013566 2 218297998 intron variant -/C ins 5
rs540653847 6 31307016 intron variant -/C delins 4.2E-03 2
rs5822105 17 75826516 downstream gene variant -/C delins 0.50 1
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs776509440 17 46096136 intron variant -/CTT;CTTT;CTTTT;CTTTTT;CTTTTTT;CTTTTTTT;CTTTTTTTT;CTTTTTTTTTT;CTTTTTTTTTTTTTTT delins 2
rs3840870 17 50184820 3 prime UTR variant -/CTTG delins 13
rs11428934 19 48640988 intron variant -/G ins 4
rs35797862 1 93272958 intron variant -/GA delins 1
rs5833013 2 102352407 intron variant -/TA delins 2
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs11319879 10 92693719 intron variant A/- delins 0.53 2
rs75802552 4 122678167 intron variant A/- delins 0.35 2
rs66538782 1 46130565 intron variant A/-;AA;AAA delins 2
rs570794153 1 198629260 intergenic variant A/-;AA;AAA delins 1
rs11405616 5 142130697 intron variant A/-;AA;AAA;AAAA delins 4
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs11654074 17 59748211 intron variant A/C snv 0.40 5
rs1036332 1 199043349 intron variant A/C snv 0.70 2
rs10455025 1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs147453535 14 23117837 intron variant A/C snv 6.3E-03 6.2E-03 2
rs2072735 1 9295413 intron variant A/C snv 0.76 2
rs77940566 6 42542864 intergenic variant A/C snv 0.21 2