Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994095 | 0.701 | 0.360 | 15 | 89327201 | missense variant | C/T | snv | 5.1E-04 | 6.7E-04 | 21 | |
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 7 | ||
rs116928232 | 0.827 | 0.120 | 10 | 89222511 | missense variant | C/G;T | snv | 1.2E-05; 9.1E-04 | 7 | ||
rs111033560 | 0.807 | 0.040 | 6 | 118559037 | stop gained | T/G | snv | 1.6E-05 | 7 | ||
rs267607277 | 0.807 | 0.120 | 14 | 90404386 | missense variant | A/G | snv | 3 | |||
rs730880082 | 0.882 | 0.120 | 6 | 7576986 | stop gained | C/G;T | snv | 3 | |||
rs12720459 | 0.807 | 0.160 | 11 | 2583535 | missense variant | C/A;G;T | snv | 3 | |||
rs587782933 | 0.827 | 0.200 | 12 | 2504526 | missense variant | G/A | snv | 2 | |||
rs79891110 | 0.807 | 0.320 | 12 | 2504944 | stop gained | G/A;T | snv | 2 | |||
rs755221106 | 0.851 | 0.040 | 17 | 50617560 | missense variant | G/A;T | snv | 4.0E-06 | 2 | ||
rs786205745 | 0.807 | 0.320 | 12 | 2504538 | missense variant | G/A;C | snv | 1 | |||
rs80315385 | 0.882 | 0.200 | 12 | 2504932 | missense variant | G/A | snv | 1 | |||
rs398124647 | 0.807 | 0.120 | 2 | 47161851 | missense variant | T/A;C | snv | 1 | |||
rs777919630 | 0.623 | 0.680 | 21 | 43062358 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
rs587777598 | 0.851 | 0.200 | 6 | 79921662 | missense variant | C/G;T | snv | 1 | |||
rs104894393 | 0.925 | 0.120 | 13 | 101726785 | missense variant | A/G | snv | 1 | |||
rs120074192 | 0.763 | 0.120 | 11 | 2527959 | missense variant | A/G | snv | 1 | |||
rs11567847 | 0.925 | 0.120 | 11 | 12937202 | missense variant | T/C | snv | 1 | |||
rs606231451 | 0.925 | 0.120 | 1 | 1535372 | missense variant | G/A | snv | 1 |