Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3021088 | 0.925 | 0.120 | MT | 5460 | missense variant | G/A | snv | 2 | |||
rs17879961 | 0.597 | 0.480 | 22 | 28725099 | missense variant | A/C;G | snv | 4.1E-03 | 53 | ||
rs2073389 | 0.925 | 0.120 | 22 | 23791306 | intron variant | C/T | snv | 0.59 | 2 | ||
rs2074733 | 0.925 | 0.120 | 22 | 30342598 | non coding transcript exon variant | T/C | snv | 0.53 | 2 | ||
rs5757573 | 0.925 | 0.120 | 22 | 39237617 | intron variant | C/T | snv | 0.57 | 2 | ||
rs5768709 | 0.925 | 0.120 | 22 | 48533757 | intron variant | A/G | snv | 0.36 | 2 | ||
rs6001516 | 0.925 | 0.120 | 22 | 39248198 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs372883 | 0.827 | 0.360 | 21 | 29345416 | 3 prime UTR variant | T/C | snv | 0.53 | 5 | ||
rs2027605 | 1.000 | 0.120 | 21 | 29354452 | intron variant | A/G | snv | 0.48 | 3 | ||
rs1153280 | 1.000 | 0.120 | 21 | 29305751 | intron variant | G/A | snv | 0.52 | 2 | ||
rs1547374 | 0.925 | 0.120 | 21 | 42358786 | downstream gene variant | A/G | snv | 0.32 | 2 | ||
rs1630747 | 0.925 | 0.120 | 21 | 34085692 | intron variant | C/A | snv | 0.69 | 2 | ||
rs2236479 | 0.925 | 0.160 | 21 | 45499218 | intron variant | G/A | snv | 0.40 | 2 | ||
rs1153287 | 1.000 | 0.120 | 21 | 29313290 | intron variant | G/A;T | snv | 1 | |||
rs1153294 | 1.000 | 0.120 | 21 | 29328775 | intron variant | T/C;G | snv | 1 | |||
rs117214 | 1.000 | 0.120 | 21 | 29348513 | intron variant | C/T | snv | 0.45 | 1 | ||
rs2832290 | 1.000 | 0.120 | 21 | 29356542 | intron variant | A/G | snv | 0.48 | 1 | ||
rs2585428 | 0.763 | 0.200 | 20 | 54170358 | intron variant | C/T | snv | 0.46 | 11 | ||
rs2762932 | 0.882 | 0.200 | 20 | 54151852 | downstream gene variant | T/C | snv | 0.17 | 3 | ||
rs757748401 | 0.925 | 0.120 | 20 | 51542465 | missense variant | C/A;T | snv | 5.2E-06 | 3 | ||
rs1810636 | 0.925 | 0.160 | 20 | 2674279 | regulatory region variant | A/C;T | snv | 2 | |||
rs6127119 | 0.925 | 0.120 | 20 | 54162543 | intron variant | C/T | snv | 0.24 | 2 | ||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs1799782 | 0.474 | 0.800 | 19 | 43553422 | missense variant | G/A | snv | 9.5E-02 | 7.0E-02 | 151 | |
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 |