Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4277405 17 63471557 upstream gene variant C/T snv 0.63 4
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 4
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs1030431 8 58399138 intergenic variant A/G;T snv 3
rs11688682 1.000 0.080 2 120590036 intergenic variant G/C snv 0.20 3
rs12627514 1.000 0.040 21 43339560 intergenic variant C/A;G;T snv 3
rs1883711 20 40551182 regulatory region variant G/C snv 2.5E-02 3
rs2760061 1 228003374 upstream gene variant T/A snv 0.55 3
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs557675 0.925 0.120 11 65799248 upstream gene variant T/A;G snv 3
rs6787344 3 186622052 intron variant G/C snv 0.19 3
rs708495 0.925 0.120 14 52302622 intergenic variant T/A snv 0.57 3
rs72801474 5 133108436 downstream gene variant G/A snv 5.2E-02 3
rs893929 4 143266227 intergenic variant G/A snv 0.42 3
rs9321485 6 135126635 intergenic variant T/C snv 0.29 3
rs11072508 1.000 0.080 15 74770056 regulatory region variant C/T snv 0.43 2
rs13210511 6 126834566 intron variant C/T snv 0.38 2
rs1560833 1 153362049 downstream gene variant G/A snv 0.22 2
rs1845034 6 50335316 intergenic variant C/T snv 0.22 2
rs2143678 6 41655295 downstream gene variant G/T snv 0.19 2
rs2569882 6 1619912 downstream gene variant T/C snv 0.50 2
rs2859814 5 32672675 intergenic variant A/G snv 0.28 2
rs2943652 2 226243730 intergenic variant C/T snv 0.65 2
rs4804517 19 7341166 TF binding site variant G/A;T snv 0.55 2