Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 8 | ||
rs760077 | 0.925 | 0.120 | 1 | 155208991 | missense variant | T/A | snv | 0.36 | 7 | ||
rs1533988 | 7 | 1253374 | intergenic variant | A/T | snv | 0.59 | 6 | ||||
rs73728279 | 1.000 | 0.080 | 7 | 151714408 | intron variant | G/A;T | snv | 4 |