Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 11 | ||
rs5050 | 0.827 | 0.200 | 1 | 230714140 | intron variant | T/C;G | snv | 7 | |||
rs2229634 | 0.851 | 0.240 | 6 | 33670403 | synonymous variant | C/A;T | snv | 4.0E-06; 0.33 | 4 | ||
rs16921209 | 0.882 | 0.160 | 10 | 20879174 | intron variant | C/G | snv | 4.6E-02 | 3 | ||
rs17076896 | 0.882 | 0.160 | 13 | 19181923 | upstream gene variant | T/C | snv | 8.3E-02 | 3 | ||
rs7637803 | 0.882 | 0.160 | 3 | 151371438 | intron variant | C/G;T | snv | 3 | |||
rs899162 | 0.882 | 0.160 | 5 | 135459219 | downstream gene variant | G/A | snv | 1.0E-01 | 3 |