Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17291650 | 12 | 50819650 | synonymous variant | A/G | snv | 6.7E-02 | 6.4E-02 | 2 | |||
rs10829156 | 10 | 18661626 | intron variant | T/C | snv | 0.79 | 2 | ||||
rs2281680 | 14 | 23563861 | splice region variant | C/T | snv | 0.18 | 0.13 | 2 | |||
rs1559040 | 2 | 54120613 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs2824292 | 0.925 | 0.080 | 21 | 17414857 | regulatory region variant | G/A | snv | 0.47 | 3 | ||
rs597503 | 18 | 6939948 | upstream gene variant | G/A;C | snv | 3 | |||||
rs10833905 | 11 | 23023046 | regulatory region variant | T/A | snv | 0.25 | 2 | ||||
rs11624056 | 14 | 87039904 | intergenic variant | A/T | snv | 8.0E-02 | 2 | ||||
rs12155623 | 8 | 48899642 | regulatory region variant | A/C;T | snv | 2 | |||||
rs17718586 | 17 | 70648048 | intergenic variant | G/T | snv | 7.1E-02 | 2 | ||||
rs1823172 | 12 | 127308069 | intergenic variant | C/T | snv | 0.17 | 2 | ||||
rs2389202 | 4 | 116333133 | intergenic variant | A/T | snv | 0.78 | 2 | ||||
rs54211 | 22 | 39291479 | upstream gene variant | A/G | snv | 0.90 | 2 | ||||
rs6716724 | 2 | 11370822 | intergenic variant | A/G | snv | 0.82 | 2 | ||||
rs6964415 | 7 | 46202985 | intergenic variant | T/A;C;G | snv | 2 |