Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs727428 | 0.882 | 0.200 | 17 | 7634474 | downstream gene variant | T/C | snv | 0.55 | 11 | ||
rs12150660 | 1.000 | 0.040 | 17 | 7618597 | intron variant | G/T | snv | 0.17 | 5 | ||
rs6258 | 1.000 | 0.040 | 17 | 7631360 | missense variant | C/A;T | snv | 5.6E-05; 4.5E-03 | 5 | ||
rs2075230 | 17 | 7583790 | 5 prime UTR variant | A/C;G | snv | 4.0E-06; 0.19 | 3 |