Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10113215 1.000 0.040 8 59219635 intergenic variant A/G snv 0.33 1
rs10512441 1.000 0.040 17 32912627 regulatory region variant C/T snv 0.21 1
rs10936538 1.000 0.040 3 167439281 downstream gene variant C/A;T snv 1
rs11658305 1.000 0.040 17 7526004 intergenic variant A/C;T snv 1
rs1370156 1.000 0.040 15 34692682 intergenic variant G/C snv 0.67 1
rs1556867 1.000 0.040 1 164244449 intergenic variant C/T snv 0.24 1
rs1585471 1.000 0.040 4 111781479 regulatory region variant A/G snv 0.30 1
rs2218817 1.000 0.040 4 111689850 regulatory region variant G/A snv 0.32 1
rs61049169 1.000 0.040 2 146131140 intergenic variant G/A;C snv 1
rs6837348 1.000 0.040 4 111787647 intergenic variant G/A snv 0.28 1
rs73157695 1.000 0.040 21 45952033 intergenic variant G/A snv 0.29 1
rs9585327 1.000 0.040 13 100037100 intergenic variant G/A snv 0.36 1
rs7162310 1.000 0.040 15 63279035 intron variant C/T snv 0.28 1
rs4948523 1.000 0.040 10 58579338 intron variant A/C snv 0.51 1
rs5022942 1.000 0.040 4 81038812 intron variant A/G snv 0.59 1
rs3760753 1.000 0.040 19 10011783 upstream gene variant G/A;T snv 1
rs34016308 1.000 0.040 14 92149397 intron variant -/TA delins 0.19 1
rs2155413 1.000 0.040 11 84923746 intron variant C/A snv 0.55 1
rs10892173 1.000 0.040 11 117801846 3 prime UTR variant C/T snv 0.38 1
rs11743810 1.000 0.040 5 138466715 intron variant C/T snv 0.50 0.48 1
rs10462070 1.000 0.040 5 44305647 intron variant A/G snv 1.2E-02 1
rs12517396 1.000 0.040 5 44359424 intron variant C/A snv 4.1E-02 1
rs201140091 1.000 0.040 10 48200198 intron variant A/-;AAAAA;AAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA delins 1
rs297589 1.000 0.040 2 156502238 intron variant T/A snv 0.65 1
rs71041628 1.000 0.040 11 105794433 intron variant GTGTGTGTGT/-;GTGT;GTGTGT;GTGTGTGT;GTGTGTGTGTGT delins 0.67 1