Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 6 | ||
rs10994359 | 0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 | 3 | ||
rs4624519 | 0.925 | 0.040 | 3 | 36821489 | intron variant | C/A;G;T | snv | 0.37 | 2 | ||
rs6550435 | 0.925 | 0.040 | 3 | 36822998 | upstream gene variant | T/G | snv | 0.38 | 2 |