Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs401681 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 9 | ||
rs31489 | 0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 | 4 | ||
rs31490 | 0.776 | 0.280 | 5 | 1344343 | splice region variant | G/A;T | snv | 0.37; 8.0E-06 | 2 | ||
rs31484 | 0.851 | 0.160 | 5 | 1337791 | intron variant | A/T | snv | 0.51 | 1 | ||
rs380286 | 0.776 | 0.200 | 5 | 1320132 | intron variant | G/A | snv | 0.47 | 1 | ||
rs421629 | 0.925 | 0.160 | 5 | 1320021 | intron variant | G/A | snv | 0.50 | 1 | ||
rs451360 | 0.827 | 0.200 | 5 | 1319565 | intron variant | C/A;T | snv | 1 | |||
rs465498 | 0.776 | 0.200 | 5 | 1325688 | non coding transcript exon variant | A/G | snv | 0.46 | 1 |