Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 3
rs4574921 0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80 3
rs9271348 0.925 0.160 6 32615965 regulatory region variant G/A snv 0.74 2
rs9302752 0.925 0.120 16 50685192 upstream gene variant T/C snv 0.68 2
rs10982385 1.000 0.040 9 114730737 intergenic variant T/G snv 0.47 1
rs13220141 1.000 0.040 6 146576497 intergenic variant A/T snv 8.2E-02 1
rs1587601 1.000 0.040 5 35254508 intergenic variant A/G snv 0.64 1
rs160451 1.000 0.040 8 89650713 intron variant T/C snv 0.56 1
rs16948876 1.000 0.040 16 50820507 intergenic variant G/A snv 6.2E-02 1
rs28490179 1.000 0.040 6 32551228 upstream gene variant C/T snv 0.81 1
rs295340 1.000 0.040 6 159164909 upstream gene variant A/G snv 0.53 1
rs34411505 1.000 0.040 16 27395368 intergenic variant A/C;G snv 1
rs383592 1.000 0.040 8 89792100 downstream gene variant C/T snv 0.58 1
rs40457 1.000 0.040 8 89811459 intergenic variant A/G snv 0.58 1
rs55894533 1.000 0.040 8 11891733 downstream gene variant A/C;T snv 1
rs58600253 1.000 0.040 10 62748144 intron variant C/T snv 5.5E-02 1
rs6807915 1.000 0.040 3 12272347 intergenic variant T/C snv 0.65 1
rs6863015 1.000 0.040 5 159416227 intron variant C/A;T snv 1
rs9567307 1.000 0.040 13 43897741 intron variant A/G snv 0.27 1
rs2221593 1.000 0.040 1 212700089 upstream gene variant C/A;G;T snv 1
rs4720118 1.000 0.040 7 33429629 intron variant T/A;C snv 1
rs3762318 0.925 0.040 1 67131436 intron variant G/A snv 0.83 3
rs2024825 1.000 0.040 1 67132294 intron variant T/A;C;G snv 1