Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs871657 | 1.000 | 0.080 | 2 | 102154881 | intron variant | C/T | snv | 0.22 | 2 | ||
rs949963 | 0.925 | 0.160 | 2 | 102153326 | intron variant | C/T | snv | 0.22 | 2 | ||
rs10166330 | 2 | 102433930 | intron variant | C/T | snv | 0.22 | 1 | ||||
rs10167431 | 2 | 102236342 | intron variant | T/C | snv | 0.55 | 1 | ||||
rs10170583 | 2 | 102358304 | intron variant | G/A | snv | 0.45 | 1 | ||||
rs10172039 | 2 | 102122325 | intron variant | C/A | snv | 0.18 | 1 | ||||
rs10172116 | 2 | 102471113 | upstream gene variant | C/G;T | snv | 1 | |||||
rs10174949 | 1.000 | 0.080 | 2 | 8302118 | non coding transcript exon variant | G/A | snv | 0.23 | 1 | ||
rs10176664 | 2 | 102359712 | intron variant | G/A;C | snv | 1 | |||||
rs10176820 | 2 | 102437960 | intron variant | T/C | snv | 0.24 | 1 | ||||
rs10177758 | 2 | 197994193 | intron variant | A/G | snv | 0.48 | 1 | ||||
rs10178214 | 2 | 102242461 | downstream gene variant | G/T | snv | 0.24 | 1 | ||||
rs10178845 | 1.000 | 0.080 | 2 | 8303673 | intron variant | G/A | snv | 0.23 | 1 | ||
rs10181785 | 2 | 102408814 | upstream gene variant | C/T | snv | 0.22 | 1 | ||||
rs10184227 | 2 | 198029581 | intron variant | C/T | snv | 0.48 | 1 | ||||
rs10184395 | 2 | 198029561 | intron variant | G/A | snv | 0.69 | 1 | ||||
rs10189897 | 2 | 197948686 | intron variant | A/G;T | snv | 1 | |||||
rs10190226 | 2 | 198036840 | intron variant | C/T | snv | 0.69 | 1 | ||||
rs10192466 | 2 | 197873295 | intron variant | G/A;C | snv | 1 | |||||
rs10196612 | 2 | 198029415 | intron variant | T/C | snv | 0.49 | 1 | ||||
rs10196961 | 2 | 197649206 | intron variant | G/A | snv | 0.47 | 1 | ||||
rs10197310 | 2 | 102403570 | downstream gene variant | T/A | snv | 0.22 | 1 | ||||
rs10198606 | 2 | 197905015 | intron variant | C/A;G;T | snv | 1 | |||||
rs10202813 | 2 | 102403280 | downstream gene variant | G/T | snv | 0.22 | 1 | ||||
rs10206714 | 2 | 198041757 | intron variant | C/A;T | snv | 1 |