Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6277 | 0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 | 36 | |
rs63751243 | 0.882 | 0.160 | 17 | 44349190 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs59115483 | 0.882 | 0.080 | 12 | 52519789 | missense variant | C/T | snv | 2.4E-05 | 7.0E-06 | 4 | |
rs556450190 | 1.000 | 0.080 | 15 | 50997380 | missense variant | G/A | snv | 2.5E-05 | 1.7E-04 | 3 | |
rs760021635 | 1.000 | 0.080 | 15 | 50958492 | missense variant | G/A | snv | 8.2E-06 | 7.0E-06 | 3 | |
rs58898021 | 0.925 | 0.160 | 2 | 219421385 | missense variant | G/C | snv | 3 | |||
rs762040846 | 1.000 | 0.080 | 17 | 41586327 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs121912476 | 1.000 | 12 | 52516824 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 2 |