Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13069000 | 3 | 66748526 | regulatory region variant | C/G | snv | 0.15 | 1 | ||||
rs7084402 | 0.925 | 0.040 | 10 | 58505644 | intergenic variant | A/G | snv | 0.51 | 1 | ||
rs10821944 | 1.000 | 0.120 | 10 | 62025330 | 3 prime UTR variant | G/T | snv | 0.66 | 1 | ||
rs11868441 | 17 | 61161860 | intron variant | A/G | snv | 0.62 | 1 | ||||
rs219778 | 0.925 | 0.120 | 21 | 36462343 | intron variant | A/G | snv | 0.31 | 1 | ||
rs2049805 | 1 | 155225189 | intron variant | T/A;C | snv | 1 | |||||
rs6026584 | 0.925 | 0.040 | 20 | 58894018 | intron variant | T/C | snv | 0.70 | 1 | ||
rs1169286 | 1.000 | 0.080 | 12 | 120981253 | intron variant | T/C | snv | 0.39 | 1 | ||
rs10767873 | 11 | 30747131 | intergenic variant | C/T | snv | 0.35 | 1 | ||||
rs10937329 | 3 | 187995930 | downstream gene variant | T/A | snv | 0.27 | 1 | ||||
rs16853722 | 3 | 169432844 | intron variant | T/C | snv | 0.11 | 1 | ||||
rs11123170 | 2 | 113221363 | intron variant | C/G | snv | 0.35 | 1 | ||||
rs7227483 | 18 | 45607165 | intron variant | A/G;T | snv | 1 | |||||
rs2206271 | 6 | 50818295 | upstream gene variant | T/A | snv | 0.32 | 1 | ||||
rs10275044 | 7 | 1234209 | intron variant | A/T | snv | 0.60 | 1 | ||||
rs17730281 | 1.000 | 0.080 | 15 | 53615751 | missense variant | G/A | snv | 0.26 | 0.22 | 1 | |
rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 2 | ||
rs12908437 | 0.882 | 0.200 | 15 | 98744146 | intron variant | T/C;G | snv | 2 | |||
rs3925584 | 1.000 | 0.080 | 11 | 30738788 | intergenic variant | T/C | snv | 0.35 | 2 | ||
rs17050272 | 0.882 | 0.120 | 2 | 120548864 | upstream gene variant | G/A | snv | 0.33 | 2 | ||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 2 | ||
rs4886755 | 0.925 | 0.120 | 15 | 76005791 | non coding transcript exon variant | A/G;T | snv | 0.49 | 3 | ||
rs1936800 | 6 | 127114919 | intron variant | C/T | snv | 0.51 | 4 | ||||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 6 | ||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 7 |