Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3923809 | 1.000 | 0.080 | 6 | 38473194 | intron variant | A/G | snv | 0.32 | 1 | ||
rs4236060 | 1.000 | 0.080 | 6 | 38502311 | intron variant | C/T | snv | 0.22 | 1 | ||
rs4714156 | 0.925 | 0.120 | 6 | 38393336 | intron variant | C/T | snv | 0.36 | 1 | ||
rs6904723 | 1.000 | 0.080 | 6 | 38468541 | intron variant | A/C;T | snv | 1 | |||
rs6923737 | 1.000 | 0.080 | 6 | 38515788 | intron variant | T/C | snv | 0.28 | 1 | ||
rs9296249 | 0.882 | 0.120 | 6 | 38398065 | intron variant | T/C | snv | 0.30 | 1 | ||
rs9357271 | 0.776 | 0.160 | 6 | 38398097 | intron variant | T/C | snv | 0.38 | 1 |