Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7916840 | 0.925 | 0.160 | 10 | 25424152 | intron variant | A/T | snv | 0.70 | 2 | ||
rs4097490 | 10 | 25497603 | intron variant | A/G | snv | 0.61 | 2 | ||||
rs1754257 | 1.000 | 0.080 | 10 | 25385685 | intron variant | G/A | snv | 0.71 | 1 | ||
rs1360123 | 10 | 25484165 | intron variant | A/G | snv | 0.44 | 1 | ||||
rs10508700 | 10 | 25532389 | intron variant | T/C | snv | 0.60 | 1 | ||||
rs4749043 | 10 | 25533431 | intron variant | A/G | snv | 0.29 | 1 | ||||
rs11014632 | 10 | 25588722 | intron variant | A/G | snv | 0.60 | 1 | ||||
rs7077800 | 10 | 25530299 | intron variant | C/T | snv | 0.53 | 1 | ||||
rs7086249 | 10 | 25522506 | intron variant | T/C | snv | 0.52 | 1 |