Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1042725 | 0.882 | 0.080 | 12 | 65964567 | 3 prime UTR variant | C/T | snv | 0.48 | 2 | ||
rs10788038 | 10 | 120117008 | intergenic variant | T/C | snv | 0.61 | 1 | ||||
rs10814916 | 0.851 | 0.200 | 9 | 4293150 | intron variant | A/C | snv | 0.57 | 3 | ||
rs10830963 | 0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 | 6 | ||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 2 | |||||
rs1151200 | 11 | 79281641 | intron variant | T/C | snv | 0.50 | 1 | ||||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 4 | ||
rs11867479 | 17 | 70094066 | intron variant | C/A;T | snv | 1 | |||||
rs12340987 | 9 | 85156012 | upstream gene variant | A/G | snv | 0.19 | 1 | ||||
rs12461110 | 19 | 55809297 | missense variant | G/A | snv | 0.32 | 0.26 | 1 | |||
rs13271368 | 8 | 125493898 | intron variant | C/T | snv | 0.18 | 1 | ||||
rs1351394 | 12 | 65958046 | 3 prime UTR variant | T/C;G | snv | 1 | |||||
rs1415701 | 6 | 130024690 | intron variant | G/A | snv | 0.31 | 1 | ||||
rs17064002 | 13 | 42996665 | upstream gene variant | C/T | snv | 1.8E-02 | 1 | ||||
rs17138114 | 6 | 4379277 | intron variant | A/G | snv | 0.10 | 1 | ||||
rs17367504 | 1.000 | 0.040 | 1 | 11802721 | intron variant | A/G | snv | 0.14 | 3 | ||
rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 1 | |
rs2282978 | 7 | 92635096 | intron variant | T/C | snv | 0.38 | 1 | ||||
rs2292626 | 0.925 | 0.120 | 10 | 122427198 | intron variant | C/T | snv | 0.46 | 1 | ||
rs2421016 | 0.925 | 0.120 | 10 | 122407996 | intron variant | C/T | snv | 0.46 | 2 | ||
rs2928148 | 15 | 41109352 | intron variant | G/A | snv | 0.44 | 1 | ||||
rs2960051 | 18 | 30276169 | intergenic variant | C/T | snv | 0.84 | 1 | ||||
rs3107997 | 18 | 30340278 | intron variant | C/T | snv | 0.21 | 1 | ||||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs339969 | 15 | 60591082 | intron variant | C/A | snv | 0.68 | 1 |