Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs138740 | 0.882 | 0.160 | 22 | 35303589 | intron variant | C/T | snv | 0.51 | 3 | ||
rs56219066 | 0.882 | 0.160 | 5 | 95907227 | intron variant | T/A;C | snv | 3 | |||
rs57104699 | 0.882 | 0.160 | 7 | 21888461 | intron variant | C/A | snv | 0.26 | 3 | ||
rs73071352 | 0.882 | 0.160 | 3 | 41786808 | intron variant | A/G | snv | 0.12 | 3 | ||
rs9848754 | 0.882 | 0.160 | 3 | 41712155 | intron variant | C/T | snv | 0.18 | 3 | ||
rs57968458 | 0.882 | 0.160 | 17 | 16916785 | intergenic variant | G/A | snv | 0.15 | 3 | ||
rs6919908 | 0.882 | 0.160 | 6 | 31277183 | non coding transcript exon variant | T/C | snv | 0.83 | 3 |