Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs142530265 20 58831332 intron variant -/A delins 4.5E-02 1
rs35787829 10 68583439 intron variant -/A delins 7.2E-02 1
rs398090202 2 24833715 intron variant -/A delins 1
rs550617350 1 118939742 intron variant -/A delins 1.6E-04 1
rs397774249 21 35293938 intron variant -/A;AA delins 0.38 1
rs397807524 15 100052239 intron variant -/AA ins 7.0E-06 1
rs140708629 21 38318057 intergenic variant -/AAA delins 1
rs71909504 20 35557937 downstream gene variant -/AAATAAT;AAT;AATTAAT delins 0.13 1
rs531971847 11 78423112 intron variant -/AATTAAA delins 1
rs2307857 5 37038415 intron variant -/ATGT delins 1
rs199957421 19 10281703 intron variant -/C delins 7.6E-04 1
rs34957094 5 88979517 intron variant -/C ins 2.0E-05 1
rs386363597 13 50657252 intron variant -/C delins 1.4E-05 1
rs397831028 5 132790397 intron variant -/C delins 0.36 1
rs34214868 15 69732152 intron variant -/C;CAAAAAC ins 1
rs11424823 5 171857638 downstream gene variant -/C;CC delins 1
rs397812377 16 3979970 intron variant -/CT delins 1
rs11450220 22 38211527 intron variant -/G delins 0.58 1
rs36013629 19 49539610 intron variant -/G delins 1
rs56937648 15 98639695 intergenic variant -/GAG delins 1
rs371273023 7 55888743 intron variant -/GCATACATACGT;GCGT;GCGTACATACATACGT;GCGTACATACCT;GCGTACATACGT delins 2.0E-05 1
rs35362712 2 120856876 intron variant -/T delins 0.60 1
rs35912034 4 124024877 downstream gene variant -/T delins 0.31 1
rs71061176 12 4269579 intron variant -/T ins 0.18 1
rs76411146 8 141386279 downstream gene variant -/T ins 0.16 1