Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6475606 | 0.882 | 0.080 | 9 | 22081851 | intron variant | C/T | snv | 0.62 | 5 | ||
rs944797 | 0.882 | 0.120 | 9 | 22115287 | intron variant | T/C;G | snv | 0.49 | 5 | ||
rs1333046 | 0.925 | 0.080 | 9 | 22124124 | intron variant | T/A | snv | 0.43 | 4 | ||
rs10738609 | 1.000 | 0.040 | 9 | 22114496 | intron variant | A/C;G;T | snv | 3 | |||
rs10757279 | 0.925 | 0.040 | 9 | 22124631 | intron variant | A/G | snv | 0.40 | 3 | ||
rs2383205 | 0.925 | 0.080 | 9 | 22060936 | intron variant | A/C;G | snv | 3 | |||
rs10217586 | 1.000 | 0.040 | 9 | 22121350 | intron variant | A/T | snv | 0.52 | 2 | ||
rs10738606 | 1.000 | 0.040 | 9 | 22088091 | intron variant | A/T | snv | 0.42 | 2 | ||
rs10757277 | 1.000 | 0.040 | 9 | 22124451 | intron variant | A/G | snv | 0.40 | 2 | ||
rs1537376 | 1.000 | 0.040 | 9 | 22116221 | intron variant | T/C | snv | 0.49 | 2 |