Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10269006 1.000 0.080 7 94758031 intergenic variant G/T snv 0.32 1
rs10871290 1.000 0.080 16 74438798 intron variant C/T snv 0.61 1
rs10923574 1.000 0.080 1 118488075 regulatory region variant A/C;T snv 1
rs11096688 1.000 0.080 2 20885650 intergenic variant T/C snv 0.86 1
rs11146838 1.000 0.080 10 38856846 intergenic variant A/T snv 1
rs11155804 1.000 0.080 6 151625017 downstream gene variant T/A snv 0.36 1
rs112319461 1.000 0.080 11 116622438 intergenic variant G/A snv 3.1E-02 1
rs11264454 1.000 0.080 1 156183252 intergenic variant A/G;T snv 1
rs113167076 1.000 0.080 8 37106253 intergenic variant G/A;C snv 1
rs113289039 1.000 0.080 6 166087861 intergenic variant -/G delins 0.35 1
rs113780580 1.000 0.080 6 27587278 intergenic variant ACACAC/-;AC;ACAC;ACACACAC;ACACACACAC;ACACACACACAC delins 1
rs113953597 1.000 0.080 2 25222417 regulatory region variant G/A snv 0.22 1
rs11462858 1.000 0.080 10 121334477 intergenic variant -/T delins 0.40 1
rs11680449 1.000 0.080 2 171513371 downstream gene variant G/A snv 0.28 1
rs11822830 1.000 0.080 11 129591121 upstream gene variant A/G snv 0.65 1
rs11903787 1.000 0.080 2 120330606 downstream gene variant G/A snv 0.30 1
rs12110303 1.000 0.080 5 91367022 downstream gene variant G/A;T snv 1
rs12189522 1.000 0.080 5 53298177 non coding transcript exon variant A/G snv 1.2E-02 1
rs12250948 1.000 0.080 10 113368732 regulatory region variant T/C snv 0.59 1
rs12479355 1.000 0.080 2 226362236 intergenic variant A/G snv 0.21 1
rs12481286 1.000 0.080 20 53671071 upstream gene variant G/A;T snv 1
rs12765365 1.000 0.080 10 63089177 intergenic variant T/C snv 2.3E-02 1
rs12870942 1.000 0.080 13 73232845 intergenic variant T/C snv 0.23 1
rs12918713 1.000 0.080 16 10609831 regulatory region variant A/C snv 5.8E-02 1
rs13183434 1.000 0.080 5 45074531 intron variant G/A snv 0.13 1