Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs112875651 | 8 | 125494452 | intron variant | G/A | snv | 0.31 | 7 | ||||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 9 | |||
rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 9 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 13 | ||
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 45 | |
rs2845885 | 11 | 64101590 | intron variant | C/T | snv | 0.87 | 5 | ||||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 10 | |||
rs4660808 | 1 | 39552837 | intron variant | C/T | snv | 0.17 | 3 | ||||
rs4738141 | 8 | 71557507 | intron variant | A/G | snv | 0.41 | 3 | ||||
rs56271783 | 11 | 64237251 | intron variant | G/A;C;T | snv | 3.6E-05; 3.7E-02 | 2 | ||||
rs605066 | 6 | 139508529 | intron variant | C/T | snv | 0.53 | 6 | ||||
rs634869 | 6 | 139510620 | intron variant | T/A;C | snv | 5 | |||||
rs718314 | 0.882 | 0.120 | 12 | 26300350 | intron variant | A/G | snv | 0.27 | 6 | ||
rs72959041 | 6 | 127133748 | intron variant | G/A | snv | 3.2E-02 | 5 | ||||
rs797486 | 13 | 50647482 | intron variant | C/A | snv | 0.85 | 2 | ||||
rs863750 | 12 | 124020897 | intron variant | C/T | snv | 0.53 | 7 | ||||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs9991328 | 4 | 88791970 | intron variant | C/T | snv | 0.53 | 5 |