Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7811265 | 0.925 | 0.120 | 7 | 73520180 | intron variant | A/G | snv | 0.23 | 5 | ||
rs2074755 | 0.807 | 0.240 | 7 | 73462836 | non coding transcript exon variant | T/C | snv | 9.2E-02 | 4 | ||
rs13244268 | 0.925 | 0.120 | 7 | 73497513 | intron variant | T/C | snv | 9.2E-02 | 3 | ||
rs10239940 | 7 | 73487060 | intron variant | A/T | snv | 2.6E-02 | 2 |