Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 8 | ||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 8 | ||
rs62435145 | 1.000 | 0.040 | 7 | 1246931 | regulatory region variant | G/T | snv | 0.51 | 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 | ||||
rs9472135 | 0.925 | 0.120 | 6 | 43842065 | intron variant | T/A;C;G | snv | 6 | |||
rs11072567 | 15 | 76006403 | intron variant | A/G | snv | 0.43 | 5 | ||||
rs128494 | 21 | 36461960 | intron variant | T/C | snv | 0.72 | 4 | ||||
rs2878889 | 18 | 48936766 | intron variant | A/C;G;T | snv | 2 |