Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17715799 | 0.882 | 0.120 | 16 | 68796608 | intron variant | A/G;T | snv | 3 | |||
rs16260 | 0.716 | 0.440 | 16 | 68737131 | upstream gene variant | C/A | snv | 0.24 | 19 | ||
rs876658932 | 0.807 | 0.400 | 16 | 68801726 | stop gained | C/G;T | snv | 7 | |||
rs587782798 | 0.807 | 0.400 | 16 | 68813322 | stop gained | C/T | snv | 7 | |||
rs7198799 | 0.882 | 0.120 | 16 | 68784487 | intron variant | C/T | snv | 0.27 | 3 | ||
rs7200690 | 0.925 | 0.080 | 16 | 68744554 | intron variant | C/T | snv | 0.23 | 2 | ||
rs869312765 | 1.000 | 0.080 | 16 | 68815697 | frameshift variant | G/- | delins | 2 | |||
rs372989292 | 1.000 | 0.080 | 16 | 68829687 | missense variant | G/A | snv | 1.2E-04 | 1.5E-04 | 1 | |
rs12185157 | 0.882 | 0.120 | 16 | 68750684 | intron variant | G/A;C;T | snv | 3 | |||
rs200932258 | 1.000 | 0.080 | 16 | 68811697 | missense variant | G/A;T | snv | 7.6E-05 | 1 | ||
rs13689 | 0.851 | 0.120 | 16 | 68834619 | 3 prime UTR variant | T/A;C;G | snv | 4 | |||
rs786202482 | 0.925 | 0.080 | 16 | 68815678 | missense variant | T/C | snv | 2.1E-05 | 2 |