Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7935082 | 1.000 | 0.040 | 11 | 60387527 | intron variant | T/C | snv | 0.62 | 2 | ||
rs10501383 | 1.000 | 0.040 | 11 | 60397054 | intron variant | C/T | snv | 5.7E-02 | 1 | ||
rs10897056 | 1.000 | 0.040 | 11 | 60398982 | intron variant | A/G | snv | 0.71 | 1 | ||
rs2233244 | 1.000 | 0.040 | 11 | 60385058 | intron variant | A/C;T | snv | 0.23; 1.2E-05 | 1 | ||
rs2241920 | 1.000 | 0.040 | 11 | 60396731 | intron variant | G/A | snv | 0.65 | 0.62 | 1 | |
rs3816270 | 1.000 | 0.040 | 11 | 60396162 | 5 prime UTR variant | T/C | snv | 0.76 | 1 | ||
rs4939352 | 1.000 | 0.040 | 11 | 60405634 | intron variant | A/G | snv | 0.67 | 1 | ||
rs7107802 | 1.000 | 0.040 | 11 | 60399149 | intron variant | T/C | snv | 0.69 | 1 | ||
rs950802 | 1.000 | 0.040 | 11 | 60385111 | synonymous variant | G/A | snv | 0.35 | 0.36 | 1 | |
rs950803 | 1.000 | 0.040 | 11 | 60385090 | splice region variant | T/A | snv | 0.64 | 0.60 | 1 |