Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs61742245 | 16 | 31094624 | missense variant | C/A;T | snv | 2.4E-03 | 2 | ||||
rs72558191 | 10 | 94947919 | missense variant | T/G | snv | 1 | |||||
rs104894542 | 16 | 31091243 | missense variant | A/C | snv | 1 | |||||
rs104894539 | 16 | 31094645 | missense variant | C/A | snv | 4.3E-06 | 1.4E-05 | 1 | |||
rs104894540 | 16 | 31094596 | missense variant | A/G | snv | 1 | |||||
rs104894541 | 16 | 31094558 | missense variant | T/C | snv | 4.1E-06 | 1 | ||||
rs72547529 | 16 | 31093399 | missense variant | C/T | snv | 2.0E-04 | 8.4E-04 | 1 | |||
rs755767348 | 16 | 31093366 | missense variant | T/A | snv | 8.0E-06 | 1 | ||||
rs770703948 | 16 | 31094654 | missense variant | C/A;G;T | snv | 8.6E-06; 4.3E-06 | 1 |