Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs539703 | 0.882 | 0.200 | 6 | 32320685 | intron variant | A/C;T | snv | 4 | |||
rs926591 | 0.882 | 0.200 | 6 | 32337913 | intron variant | C/A | snv | 0.33 | 4 | ||
rs4959093 | 0.882 | 0.200 | 6 | 32345320 | intron variant | T/C | snv | 0.33 | 4 | ||
rs574710 | 0.882 | 0.200 | 6 | 32320413 | intron variant | T/C | snv | 0.34 | 4 | ||
rs9268402 | 0.827 | 0.200 | 6 | 32373576 | intron variant | G/A | snv | 0.45 | 4 | ||
rs9368716 | 0.882 | 0.200 | 6 | 32338313 | intron variant | G/A | snv | 0.39 | 4 | ||
rs3129900 | 0.882 | 0.200 | 6 | 32338202 | intron variant | G/T | snv | 0.83 | 3 | ||
rs6907322 | 1.000 | 0.080 | 6 | 32357168 | intron variant | G/A | snv | 0.25 | 2 | ||
rs910050 | 0.925 | 0.120 | 6 | 32347877 | intron variant | G/C | snv | 0.42 | 2 | ||
rs9268302 | 1.000 | 0.080 | 6 | 32357040 | intron variant | C/T | snv | 0.29 | 2 | ||
rs544358 | 0.925 | 0.120 | 6 | 32305381 | intron variant | G/C | snv | 0.33 | 2 |