Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9303521 | 0.925 | 0.120 | 17 | 45727828 | intron variant | T/C;G | snv | 0.60 | 5 | ||
rs12938031 | 0.851 | 0.160 | 17 | 45777136 | intron variant | A/G | snv | 0.26 | 4 | ||
rs1724422 | 1.000 | 0.040 | 17 | 45699947 | intron variant | A/G | snv | 0.47 | 2 | ||
rs34186148 | 1.000 | 0.040 | 17 | 45777289 | intron variant | G/A;C | snv | 0.31 | 2 | ||
rs35909029 | 1.000 | 0.040 | 17 | 45774132 | intron variant | T/A;C;G | snv | 2 | |||
rs62057061 | 1.000 | 0.040 | 17 | 45779273 | intron variant | C/G | snv | 0.14 | 2 | ||
rs7225384 | 1.000 | 0.040 | 17 | 45731730 | non coding transcript exon variant | C/G | snv | 0.39 | 2 |