Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2517955 | 1.000 | 0.080 | 17 | 39687428 | intron variant | C/T | snv | 0.51 | 1 | ||
rs12150298 | 1.000 | 0.080 | 17 | 39678288 | intron variant | T/C | snv | 0.58 | 1 | ||
rs1565922 | 1.000 | 0.080 | 17 | 39674782 | intron variant | A/G;T | snv | 1 | |||
rs2941503 | 1.000 | 0.080 | 17 | 39672492 | missense variant | A/G | snv | 0.64 | 1 | ||
rs2941504 | 1.000 | 0.080 | 17 | 39674647 | synonymous variant | A/G | snv | 0.67 | 0.64 | 1 |