Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs597503 | 18 | 6939948 | upstream gene variant | G/A;C | snv | 3 | |||||
rs10183640 | 2 | 157923692 | intron variant | G/A | snv | 0.31 | 2 | ||||
rs10765792 | 11 | 96133536 | intron variant | G/C | snv | 0.10 | 2 | ||||
rs10829156 | 10 | 18661626 | intron variant | T/C | snv | 0.79 | 2 | ||||
rs10833905 | 11 | 23023046 | regulatory region variant | T/A | snv | 0.25 | 2 | ||||
rs11187837 | 10 | 94276223 | intron variant | T/C | snv | 8.4E-02 | 2 | ||||
rs11624056 | 14 | 87039904 | intergenic variant | A/T | snv | 8.0E-02 | 2 | ||||
rs12155623 | 8 | 48899642 | regulatory region variant | A/C;T | snv | 2 | |||||
rs12189362 | 5 | 153677988 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs12429889 | 13 | 74168185 | intergenic variant | T/C | snv | 0.29 | 2 | ||||
rs13022357 | 2 | 159213245 | intron variant | A/G | snv | 0.83 | 2 | ||||
rs1559040 | 2 | 54120613 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs16866933 | 2 | 179701951 | intron variant | G/A | snv | 9.3E-02 | 2 | ||||
rs16872085 | 8 | 104945312 | intron variant | A/G | snv | 7.6E-02 | 2 | ||||
rs16942421 | 18 | 26576461 | intron variant | G/A;T | snv | 2 | |||||
rs17291650 | 12 | 50819650 | synonymous variant | A/G | snv | 6.7E-02 | 6.4E-02 | 2 | |||
rs17718586 | 17 | 70648048 | intergenic variant | G/T | snv | 7.1E-02 | 2 | ||||
rs1823172 | 12 | 127308069 | intergenic variant | C/T | snv | 0.17 | 2 | ||||
rs2281680 | 14 | 23563861 | splice region variant | C/T | snv | 0.18 | 0.13 | 2 | |||
rs2389202 | 4 | 116333133 | intergenic variant | A/T | snv | 0.78 | 2 | ||||
rs2982694 | 6 | 151964552 | intron variant | G/T | snv | 0.86 | 2 | ||||
rs4621553 | 5 | 113694467 | intergenic variant | G/A | snv | 0.78 | 2 | ||||
rs4665058 | 2 | 159333698 | intron variant | A/C | snv | 0.90 | 2 | ||||
rs54211 | 22 | 39291479 | upstream gene variant | A/G | snv | 0.90 | 2 | ||||
rs62641689 | 15 | 73323818 | missense variant | C/A;T | snv | 3.2E-03 | 2 |