Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs340561 1.000 0.080 13 72274018 intergenic variant G/T snv 0.23 1
rs35041767 1.000 0.080 9 9261737 intron variant -/C ins 1
rs35987657 1.000 0.080 3 130816723 upstream gene variant A/G snv 0.29 1
rs365032 1.000 0.080 20 64164052 intron variant A/G snv 0.26 1
rs3784709 1.000 0.080 15 67779937 intron variant C/T snv 0.36 1
rs3923809 1.000 0.080 6 38473194 intron variant A/G snv 0.32 1
rs4236060 1.000 0.080 6 38502311 intron variant C/T snv 0.22 1
rs4489954 1.000 0.080 15 67779737 intron variant T/A;G snv 1
rs45544231 1.000 0.080 16 52598818 intron variant G/C;T snv 1
rs4626664 1.000 0.080 9 9261737 intron variant G/A snv 0.20 1
rs4784226 1.000 0.080 16 52549231 upstream gene variant C/T snv 0.20 1
rs61192259 1.000 0.080 6 38486186 intron variant C/A snv 0.50 1
rs62535767 1.000 0.080 9 9290311 intron variant C/T snv 0.25 1
rs6494696 1.000 0.080 15 67810868 downstream gene variant G/A;C snv 1
rs6747972 1.000 0.080 2 67843093 intergenic variant A/G snv 0.65 1
rs6904723 1.000 0.080 6 38468541 intron variant A/C;T snv 1
rs6923737 1.000 0.080 6 38515788 intron variant T/C snv 0.28 1
rs7881785 1.000 0.080 X 42995357 upstream gene variant A/G snv 1
rs80319144 1.000 0.080 2 158343323 intron variant C/T snv 0.18 1
rs868036 1.000 0.080 15 67762675 intron variant T/A snv 0.62 1
rs9390170 1.000 0.080 6 144530548 intron variant G/C snv 0.11 1
rs996064 1.000 0.080 15 35916797 upstream gene variant A/T snv 3.7E-02 1
rs2300478 0.851 0.120 2 66554321 intron variant T/G snv 0.21 6
rs3794087 0.851 0.120 11 35308068 intron variant G/T snv 0.20 6
rs41305272 0.851 0.120 15 67807105 3 prime UTR variant C/T snv 2.4E-02 6