Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 22 | ||
rs1333040 | 0.732 | 0.280 | 9 | 22083405 | intron variant | C/G;T | snv | 15 | |||
rs10757272 | 0.851 | 0.160 | 9 | 22088261 | intron variant | C/T | snv | 0.41 | 6 | ||
rs496892 | 0.827 | 0.160 | 9 | 22024352 | intron variant | C/T | snv | 0.40 | 6 | ||
rs6475606 | 0.882 | 0.080 | 9 | 22081851 | intron variant | C/T | snv | 0.62 | 5 | ||
rs10733376 | 1.000 | 0.080 | 9 | 22114470 | intron variant | G/C | snv | 0.64 | 3 |