Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 5
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 4
rs148696809 0.851 0.160 6 28966575 downstream gene variant T/C snv 5.3E-02 4
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 4