Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 41 | |
rs11542041 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 23 | ||
rs5742904 | 0.689 | 0.280 | 2 | 21006288 | missense variant | C/A;T | snv | 2.8E-04 | 7.3E-04 | 22 | |
rs267606661 | 0.763 | 0.120 | 19 | 44909101 | missense variant | C/G;T | snv | 3.9E-04; 1.0E-05 | 10 | ||
rs573658040 | 0.790 | 0.200 | 19 | 44908705 | missense variant | C/G;T | snv | 6.3E-06 | 9 | ||
rs769455 | 0.827 | 0.120 | 19 | 44908783 | missense variant | C/T | snv | 1.4E-03 | 6.9E-03 | 8 | |
rs879254693 | 0.807 | 0.160 | 19 | 11107424 | missense variant | T/A;C;G | snv | 7 | |||
rs121918393 | 0.851 | 0.120 | 19 | 44908756 | missense variant | C/A;T | snv | 1.3E-05; 9.0E-05 | 6 | ||
rs121918394 | 0.882 | 0.080 | 19 | 44908786 | missense variant | A/C;G | snv | 6.5E-06 | 5 | ||
rs267606664 | 0.851 | 0.120 | 19 | 44908730 | missense variant | G/A;C | snv | 1.6E-04; 6.3E-06 | 5 | ||
rs199768005 | 0.882 | 0.160 | 19 | 44909057 | missense variant | T/A | snv | 4.5E-04 | 4.9E-04 | 4 | |
rs387906567 | 0.882 | 0.200 | 19 | 44908774 | missense variant | C/G;T | snv | 6.3E-06 | 4 | ||
rs121918397 | 0.882 | 0.200 | 19 | 44908784 | missense variant | G/A;C | snv | 6.5E-06 | 3 | ||
rs879254728 | 0.882 | 0.080 | 19 | 11107511 | missense variant | T/C;G | snv | 3 | |||
rs1466963971 | 0.925 | 0.120 | 19 | 44908640 | missense variant | T/G | snv | 4.5E-06 | 2 | ||
rs201672011 | 1.000 | 0.080 | 19 | 44907807 | missense variant | G/A | snv | 1.2E-04 | 4.8E-04 | 2 | |
rs121912502 | 0.925 | 0.080 | 15 | 58548387 | missense variant | C/T | snv | 1.0E-03 | 7.5E-04 | 2 | |
rs11542037 | 1.000 | 0.080 | 19 | 44908657 | missense variant | C/A;T | snv | 5.2E-06 | 1 | ||
rs121918396 | 1.000 | 0.080 | 19 | 44908979 | stop gained | G/A | snv | 1.6E-05 | 3.5E-05 | 1 | |
rs397514253 | 1.000 | 0.080 | 19 | 44908531 | splice acceptor variant | A/G | snv | 1 | |||
rs760473480 | 1.000 | 0.080 | 11 | 35189846 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
rs757292254 | 1.000 | 0.080 | 19 | 11105453 | missense variant | C/T | snv | 4.0E-06 | 1 |