Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3746544 | 0.790 | 0.120 | 20 | 10306436 | 3 prime UTR variant | G/T | snv | 0.68 | 10 | ||
rs3796863 | 0.790 | 0.160 | 4 | 15848363 | intron variant | G/T | snv | 0.41 | 8 | ||
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 3 | ||
rs4307059 | 0.882 | 0.080 | 5 | 25967594 | intron variant | T/A;C | snv | 5 | |||
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs6150410 | 0.925 | 0.040 | 7 | 155454910 | intron variant | CGCATCCCC/-;CGCATCCCCCGCATCCCC | delins | 0.28 | 2 | ||
rs6311 | 0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 | 41 | ||
rs6735330 | 0.925 | 0.040 | 2 | 61504343 | intron variant | G/A | snv | 0.18 | 2 | ||
rs6950765 | 0.925 | 0.040 | 7 | 117281176 | intron variant | C/G | snv | 0.64 | 2 | ||
rs7294536 | 0.925 | 0.040 | 12 | 63154312 | upstream gene variant | T/C | snv | 0.26 | 2 | ||
rs736707 | 0.851 | 0.040 | 7 | 103489956 | intron variant | A/G | snv | 0.30 | 6 | ||
rs756472 | 0.925 | 0.040 | 16 | 14185624 | intron variant | G/A | snv | 0.24 | 2 | ||
rs7608798 | 0.925 | 0.040 | 2 | 162033707 | intron variant | G/A | snv | 0.35 | 2 | ||
rs768913131 | 0.925 | 0.040 | 2 | 50552821 | missense variant | G/A | snv | 3 | |||
rs7794745 | 0.851 | 0.040 | 7 | 146792514 | intron variant | A/T | snv | 0.49 | 6 | ||
rs779867 | 0.776 | 0.120 | 3 | 7442784 | intron variant | T/C;G | snv | 9 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs747756965 | 0.925 | 0.040 | 6 | 38775924 | missense variant | T/A;C | snv | 4.0E-06 | 2 | ||
rs73598374 | 0.790 | 0.280 | 20 | 44651586 | missense variant | C/A;G;T | snv | 7.1E-06; 6.2E-02 | 8 | ||
rs1800561 | 0.807 | 0.240 | 4 | 15824935 | missense variant | C/A;T | snv | 8.0E-06; 4.4E-04 | 7 | ||
rs751945904 | 0.925 | 0.040 | X | 5893158 | missense variant | G/A | snv | 1.1E-05 | 2 | ||
rs3747334 | 0.925 | 0.040 | X | 5893489 | synonymous variant | G/A;C;T | snv | 1.2E-05; 6.7E-03 | 3 | ||
rs362691 | 0.882 | 0.120 | 7 | 103610714 | missense variant | G/A;C;T | snv | 1.2E-05; 0.12 | 3 | ||
rs201551401 | 0.925 | 0.040 | 7 | 124746694 | missense variant | C/T | snv | 6.4E-05 | 1.4E-05 | 3 |