Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs72761442 | 1.000 | 0.040 | 5 | 61400496 | intron variant | A/G | snv | 0.18 | 2 | ||
rs13179617 | 5 | 61527343 | intron variant | G/T | snv | 0.38 | 1 | ||||
rs10223052 | 5 | 61504509 | intron variant | A/G | snv | 0.73 | 1 | ||||
rs78922867 | 5 | 61501931 | intron variant | G/C | snv | 8.5E-03 | 1 | ||||
rs142089946 | 1.000 | 0.040 | 5 | 61495766 | intron variant | C/G | snv | 3.3E-02 | 1 | ||
rs7709645 | 1.000 | 0.040 | 5 | 61435631 | intron variant | G/A;C | snv | 1 | |||
rs7719676 | 1.000 | 0.040 | 5 | 61441122 | intron variant | A/G;T | snv | 1 | |||
rs4490539 | 5 | 61389930 | intron variant | A/G | snv | 0.31 | 1 | ||||
rs74419120 | 5 | 61447591 | intron variant | C/G;T | snv | 1 | |||||
rs74320437 | 5 | 61447778 | intron variant | C/T | snv | 0.17 | 1 | ||||
rs7714712 | 5 | 61436725 | intron variant | C/A | snv | 0.37 | 1 | ||||
rs7720894 | 5 | 61438106 | intron variant | G/C | snv | 0.63 | 1 | ||||
rs6449533 | 5 | 61426817 | intron variant | T/C | snv | 0.36 | 1 |