Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11557467 | 0.851 | 0.200 | 17 | 39872381 | missense variant | G/T | snv | 0.45 | 0.45 | 4 | |
rs11078925 | 0.925 | 0.160 | 17 | 39868955 | intron variant | T/C | snv | 0.36 | 3 | ||
rs11557466 | 0.925 | 0.160 | 17 | 39868373 | synonymous variant | C/T | snv | 0.40 | 0.36 | 3 | |
rs11870965 | 0.925 | 0.160 | 17 | 39873952 | intron variant | T/A | snv | 0.40 | 3 | ||
rs12936231 | 0.925 | 0.160 | 17 | 39872867 | intron variant | C/G;T | snv | 3 | |||
rs1054609 | 0.925 | 0.160 | 17 | 39877024 | 3 prime UTR variant | A/C | snv | 0.40 | 2 | ||
rs4795397 | 0.925 | 0.160 | 17 | 39867492 | upstream gene variant | A/G | snv | 0.38 | 2 | ||
rs12150079 | 0.807 | 0.280 | 17 | 39869164 | intron variant | G/A | snv | 0.24 | 1 |