Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs767910122 | 0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 | 17 | ||
rs794728448 | 0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins | 17 | |||
rs120074192 | 0.763 | 0.120 | 11 | 2527959 | missense variant | A/G | snv | 10 | |||
rs16847548 | 0.807 | 0.120 | 1 | 162065484 | upstream gene variant | T/C | snv | 0.22 | 8 | ||
rs116840778 | 0.882 | 0.200 | 3 | 8733956 | missense variant | G/A;C | snv | 7 | |||
rs12720459 | 0.807 | 0.160 | 11 | 2583535 | missense variant | C/A;G;T | snv | 7 | |||
rs199472709 | 0.790 | 0.120 | 11 | 2572021 | missense variant | G/A;T | snv | 7 | |||
rs121912504 | 0.851 | 0.200 | 7 | 150951711 | missense variant | G/A | snv | 6 | |||
rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 6 | |||
rs199472795 | 0.807 | 0.120 | 11 | 2775984 | missense variant | C/T | snv | 7.0E-06 | 6 | ||
rs267607277 | 0.807 | 0.120 | 14 | 90404386 | missense variant | A/G | snv | 6 | |||
rs398124647 | 0.807 | 0.120 | 2 | 47161851 | missense variant | T/A;C | snv | 6 | |||
rs786205745 | 0.807 | 0.320 | 12 | 2504538 | missense variant | G/A;C | snv | 6 | |||
rs79891110 | 0.807 | 0.320 | 12 | 2504944 | stop gained | G/A;T | snv | 6 | |||
rs199472687 | 0.827 | 0.120 | 11 | 2527962 | missense variant | G/A | snv | 5 | |||
rs199472730 | 0.882 | 0.120 | 11 | 2572895 | missense variant | C/G;T | snv | 5 | |||
rs199472921 | 0.882 | 0.120 | 7 | 150951712 | missense variant | C/G;T | snv | 5 | |||
rs199472936 | 0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv | 5 | |||
rs28928905 | 0.851 | 0.120 | 7 | 150952514 | missense variant | C/G;T | snv | 5 | |||
rs587782933 | 0.827 | 0.200 | 12 | 2504526 | missense variant | G/A | snv | 5 | |||
rs120074189 | 0.851 | 0.120 | 11 | 2778003 | missense variant | C/T | snv | 4 | |||
rs121912507 | 0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv | 4 | |||
rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 4 | |||
rs199473401 | 0.925 | 0.120 | 11 | 2570722 | missense variant | T/C | snv | 4 | |||
rs199473604 | 0.882 | 0.120 | 3 | 38560394 | missense variant | G/T | snv | 4 |