Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9277557 | 1.000 | 0.080 | 6 | 33088917 | 3 prime UTR variant | T/C | snv | 0.25 | 1 | ||
rs9277554 | 0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 | 7 | ||
rs9277551 | 1.000 | 0.080 | 6 | 33087717 | 3 prime UTR variant | G/A;T | snv | 1 | |||
rs9277550 | 0.925 | 0.200 | 6 | 33087710 | 3 prime UTR variant | T/C | snv | 0.38 | 2 | ||
rs9277549 | 1.000 | 0.080 | 6 | 33087642 | 3 prime UTR variant | A/G | snv | 0.38 | 1 | ||
rs9277547 | 0.925 | 0.200 | 6 | 33087590 | 3 prime UTR variant | C/A | snv | 0.38 | 2 | ||
rs9277546 | 0.925 | 0.200 | 6 | 33087569 | 3 prime UTR variant | T/G | snv | 0.38 | 2 | ||
rs9277542 | 0.851 | 0.280 | 6 | 33087470 | 3 prime UTR variant | T/A;C | snv | 4 | |||
rs9277541 | 0.925 | 0.200 | 6 | 33087381 | 3 prime UTR variant | A/G;T | snv | 2 | |||
rs9277540 | 0.925 | 0.200 | 6 | 33087346 | 3 prime UTR variant | A/G | snv | 0.38 | 2 | ||
rs9277538 | 0.925 | 0.200 | 6 | 33087270 | 3 prime UTR variant | A/G | snv | 0.38 | 2 | ||
rs9277535 | 0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 | 13 | ||
rs9277534 | 0.790 | 0.280 | 6 | 33087030 | 3 prime UTR variant | A/G | snv | 0.38 | 7 | ||
rs9277533 | 0.925 | 0.200 | 6 | 33086944 | 3 prime UTR variant | C/T | snv | 0.38 | 2 | ||
rs9277515 | 0.925 | 0.200 | 6 | 33086491 | intron variant | C/A;T | snv | 8.3E-03; 7.4E-06 | 2 | ||
rs9277495 | 1.000 | 0.080 | 6 | 33086294 | intron variant | G/C | snv | 0.38 | 1 | ||
rs9277492 | 0.925 | 0.200 | 6 | 33086205 | intron variant | G/A;C | snv | 4.4E-06; 0.28 | 2 | ||
rs9277488 | 1.000 | 0.080 | 6 | 33086129 | intron variant | G/T | snv | 0.38 | 1 | ||
rs9277480 | 1.000 | 0.080 | 6 | 33086035 | intron variant | A/G | snv | 0.25 | 1 | ||
rs9277479 | 0.925 | 0.200 | 6 | 33086012 | intron variant | A/G | snv | 0.38 | 2 | ||
rs9277477 | 0.925 | 0.200 | 6 | 33085995 | intron variant | G/A;T | snv | 2 | |||
rs9277472 | 1.000 | 0.080 | 6 | 33085946 | intron variant | T/C | snv | 0.31 | 0.38 | 1 | |
rs9277471 | 1.000 | 0.080 | 6 | 33085905 | missense variant | G/A;C | snv | 0.32; 4.1E-06 | 1 | ||
rs9277469 | 0.925 | 0.200 | 6 | 33085691 | intron variant | G/T | snv | 0.38 | 2 | ||
rs9277468 | 0.925 | 0.200 | 6 | 33085678 | intron variant | C/T | snv | 0.38 | 2 |