Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2234767 | 0.649 | 0.280 | 10 | 88989499 | intron variant | G/A;T | snv | 0.15 | 30 | ||
rs16754 | 0.732 | 0.240 | 11 | 32396399 | synonymous variant | T/C | snv | 0.24; 4.0E-06 | 0.17 | 15 | |
rs10821936 | 0.742 | 0.200 | 10 | 61963818 | intron variant | C/T | snv | 0.69 | 11 | ||
rs7089424 | 0.752 | 0.200 | 10 | 61992400 | intron variant | T/G | snv | 0.32 | 10 | ||
rs1057519753 | 0.763 | 0.120 | 1 | 64846664 | missense variant | C/A | snv | 9 | |||
rs7073837 | 0.851 | 0.120 | 10 | 61940136 | intron variant | A/C | snv | 0.58 | 0.64 | 4 | |
rs2393726 | 0.925 | 0.040 | 10 | 62094648 | 3 prime UTR variant | A/G | snv | 3.9E-02 | 2 | ||
rs6415872 | 0.925 | 0.040 | 10 | 61900930 | upstream gene variant | G/A | snv | 0.51 | 2 |