Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 1
rs16867808 1.000 0.040 6 27495905 intron variant T/C snv 6.6E-02 1
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 1
rs1842896 1.000 0.040 4 155590307 intergenic variant G/T snv 0.50 1
rs2064092 1.000 0.040 6 27543592 intergenic variant C/A snv 0.13 1
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 1
rs2123536 1.000 0.040 2 19745816 intergenic variant T/A;C snv 1
rs2129035 1.000 0.040 8 109831384 intergenic variant C/A snv 0.38 1
rs2219939 1.000 0.040 15 78737381 downstream gene variant G/A snv 0.53 1
rs2531815 1.000 0.040 6 28468283 intergenic variant C/T snv 0.44 1
rs2567446 1.000 0.040 15 95720753 intron variant A/G snv 0.62 1
rs2596551 1.000 0.040 6 31364462 upstream gene variant A/C snv 0.16 1
rs2743941 1.000 0.040 6 29787674 upstream gene variant T/C;G snv 1
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 1
rs4143832 0.925 0.080 5 132527285 intron variant T/G snv 0.76 1
rs4803770 0.925 0.120 19 44924096 upstream gene variant C/G snv 0.33 1
rs6789378 1.000 0.040 3 162449608 intergenic variant G/A snv 0.67 1
rs68191 1.000 0.040 6 33512961 regulatory region variant T/C;G snv 1
rs6903982 1.000 0.040 6 27577965 intergenic variant T/C;G snv 1
rs6910968 1.000 0.040 6 27936403 upstream gene variant C/T snv 0.13 1
rs6911476 1.000 0.040 6 26612135 non coding transcript exon variant C/T snv 0.10 1
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 1
rs7278845 1.000 0.040 21 34265162 intron variant A/G snv 0.14 1
rs7323893 1.000 0.040 13 88052451 intergenic variant T/C snv 2.6E-02 1
rs7356849 1.000 0.040 6 26396511 downstream gene variant T/C snv 0.29 1