Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1136410 | 0.559 | 0.760 | 1 | 226367601 | missense variant | A/G | snv | 0.21 | 0.15 | 70 | |
rs8679 | 0.790 | 0.200 | 1 | 226360853 | 3 prime UTR variant | A/G | snv | 0.16 | 7 | ||
rs1805404 | 0.882 | 0.200 | 1 | 226402257 | missense variant | G/A;C | snv | 0.22; 4.0E-06 | 3 | ||
rs1805414 | 0.925 | 0.080 | 1 | 226385663 | synonymous variant | A/G | snv | 0.43 | 0.42 | 2 | |
rs2230484 | 0.925 | 0.080 | 1 | 226383066 | missense variant | G/A | snv | 3.7E-03 | 3.3E-03 | 2 | |
rs4653734 | 0.925 | 0.080 | 1 | 226407688 | intron variant | C/A;G | snv | 2 | |||
rs907187 | 0.925 | 0.080 | 1 | 226407946 | 5 prime UTR variant | C/G;T | snv | 0.21; 4.1E-06 | 2 |