Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 10 | ||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 9 | |||
rs9940128 | 0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 | 6 | ||
rs9930506 | 0.776 | 0.360 | 16 | 53796553 | intron variant | A/G | snv | 0.36 | 5 | ||
rs11075985 | 1.000 | 0.080 | 16 | 53771295 | intron variant | C/A | snv | 0.42 | 2 | ||
rs9923544 | 1.000 | 0.080 | 16 | 53768073 | intron variant | C/T | snv | 0.42 | 2 | ||
rs9302652 | 1.000 | 0.080 | 16 | 53832063 | intron variant | C/T | snv | 0.74 | 1 |