Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61751306 | 1.000 | 0.080 | 12 | 5949195 | missense variant | A/C | snv | 1 | |||
rs61751305 | 1.000 | 0.080 | 12 | 5949823 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs61751298 | 1.000 | 0.080 | 12 | 5969304 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs61751296 | 0.925 | 0.080 | 12 | 5969337 | stop gained | G/A | snv | 1.6E-05 | 1.4E-05 | 2 | |
rs61750630 | 0.925 | 0.080 | 12 | 5981988 | missense variant | C/A | snv | 2 | |||
rs61750615 | 1.000 | 0.080 | 12 | 5994484 | missense variant | G/A;T | snv | 1.3E-02 | 1 | ||
rs61750612 | 0.882 | 0.080 | 12 | 6013544 | stop gained | G/A;T | snv | 1.6E-05 | 3 | ||
rs61750598 | 0.925 | 0.080 | 12 | 6018404 | missense variant | C/T | snv | 4.1E-04 | 1.7E-04 | 2 | |
rs61750595 | 0.882 | 0.080 | 12 | 6018443 | stop gained | G/A;T | snv | 5.6E-05 | 3 | ||
rs61750086 | 1.000 | 0.080 | 12 | 6019050 | stop gained | G/C;T | snv | 1 | |||
rs61748497 | 0.851 | 0.080 | 12 | 6025624 | missense variant | A/G | snv | 4 | |||
rs62643632 | 0.925 | 0.080 | 12 | 6044298 | frameshift variant | G/-;GG | delins | 6.3E-05 | 3 | ||
rs1063856 | 0.763 | 0.400 | 12 | 6044368 | missense variant | T/C;G | snv | 0.31 | 14 | ||
rs62643626 | 1.000 | 0.080 | 12 | 6071322 | missense variant | C/A | snv | 1 | |||
rs61753998 | 1.000 | 0.080 | 12 | 6075386 | missense variant | A/G;T | snv | 1 | |||
rs61753997 | 0.882 | 0.080 | 12 | 6075392 | missense variant | G/A | snv | 2.8E-05; 8.0E-06 | 4.2E-05 | 3 | |
rs958629333 | 1.000 | 0.080 | 12 | 6121245 | missense variant | A/G | snv | 1 |