Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs210987 | 0.925 | 0.080 | 5 | 162108749 | intron variant | C/T | snv | 0.54 | 2 | ||
rs211014 | 0.925 | 0.080 | 5 | 162149412 | 3 prime UTR variant | C/A | snv | 0.30 | 2 | ||
rs211037 | 0.742 | 0.240 | 5 | 162101274 | synonymous variant | C/T | snv | 0.28 | 0.31 | 14 | |
rs2292096 | 0.925 | 0.040 | 1 | 200857641 | 3 prime UTR variant | A/G | snv | 0.14 | 2 | ||
rs2422106 | 1.000 | 5 | 162134797 | intron variant | G/A;T | snv | 1 | ||||
rs401750 | 0.925 | 0.040 | 5 | 162155655 | 3 prime UTR variant | C/T | snv | 0.43 | 2 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs7103411 | 0.752 | 0.160 | 11 | 27678578 | intron variant | C/T | snv | 0.82 | 15 | ||
rs7127507 | 0.827 | 0.080 | 11 | 27693337 | intron variant | T/C | snv | 0.34 | 6 |