Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1033180 | 1.000 | 0.080 | 6 | 383546 | regulatory region variant | C/T | snv | 5.4E-02 | 1 | ||
rs10886159 | 1.000 | 0.080 | 10 | 117854099 | intergenic variant | T/C | snv | 0.25 | 1 | ||
rs10903122 | 0.882 | 0.200 | 1 | 24977085 | intergenic variant | A/G | snv | 0.56 | 1 | ||
rs12142280 | 1.000 | 0.080 | 1 | 172895512 | intron variant | T/A | snv | 0.21 | 1 | ||
rs12727642 | 1.000 | 0.080 | 1 | 7986612 | upstream gene variant | C/A | snv | 0.12 | 1 | ||
rs13132933 | 0.925 | 0.200 | 4 | 122089432 | upstream gene variant | T/C | snv | 0.22 | 1 | ||
rs1378938 | 1.000 | 0.080 | 15 | 74804102 | downstream gene variant | T/A;C | snv | 1 | |||
rs2097282 | 1.000 | 0.080 | 3 | 46336534 | intergenic variant | C/T | snv | 0.68 | 1 | ||
rs2157453 | 1.000 | 0.080 | 1 | 172894808 | intron variant | G/A | snv | 0.31 | 1 | ||
rs2187670 | 1.000 | 0.080 | 3 | 46325463 | intergenic variant | T/C | snv | 0.81 | 1 | ||
rs231804 | 0.925 | 0.200 | 2 | 203843923 | intergenic variant | C/T | snv | 0.60 | 1 | ||
rs424232 | 0.882 | 0.240 | 6 | 32240547 | intergenic variant | C/A;T | snv | 1 | |||
rs4558075 | 1.000 | 0.080 | 10 | 6359663 | intergenic variant | C/A;G;T | snv | 1 | |||
rs4899260 | 1.000 | 0.080 | 14 | 68811487 | intergenic variant | C/T | snv | 0.28 | 1 | ||
rs5979785 | 0.925 | 0.160 | X | 12953405 | intergenic variant | C/T | snv | 1 | |||
rs62184863 | 1.000 | 0.080 | 2 | 203819074 | intergenic variant | G/C | snv | 6.2E-02 | 1 | ||
rs6822844 | 0.689 | 0.520 | 4 | 122588266 | regulatory region variant | G/T | snv | 0.10 | 1 | ||
rs7104791 | 1.000 | 0.080 | 11 | 111326133 | downstream gene variant | T/A;C | snv | 1 | |||
rs859715 | 1.000 | 0.080 | 1 | 172790982 | intron variant | A/T | snv | 0.36 | 1 | ||
rs9286879 | 0.851 | 0.200 | 1 | 172893094 | intron variant | A/G | snv | 0.32 | 1 | ||
rs971290 | 1.000 | 0.080 | 14 | 68805252 | intergenic variant | C/A;G;T | snv | 1 | |||
rs9792269 | 0.882 | 0.200 | 8 | 128252343 | intergenic variant | A/C;G | snv | 1 | |||
rs8081319 | 1.000 | 0.080 | 17 | 37374139 | intron variant | A/G | snv | 6.8E-02 | 1 | ||
rs11712165 | 0.882 | 0.200 | 3 | 119399949 | intron variant | T/G | snv | 0.30 | 1 | ||
rs61579022 | 1.000 | 0.080 | 3 | 119404431 | intron variant | G/A | snv | 0.30 | 1 |