Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs2165241 | 0.716 | 0.360 | 15 | 73929861 | intron variant | T/C | snv | 0.60 | 15 | ||
rs3825942 | 0.716 | 0.320 | 15 | 73927241 | missense variant | G/A;C;T | snv | 0.18; 4.5E-06 | 15 | ||
rs1900004 | 0.827 | 0.040 | 10 | 68241124 | intron variant | C/T | snv | 0.39 | 5 |