Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7148590 | 14 | 65006478 | intron variant | G/A | snv | 0.57 | 3 | ||||
rs2120019 | 15 | 75041843 | intron variant | T/C | snv | 0.31 | 2 | ||||
rs11232535 | 11 | 81217766 | intron variant | T/C | snv | 0.15 | 1 | ||||
rs11763353 | 7 | 15591246 | intergenic variant | A/G | snv | 0.21 | 1 | ||||
rs1532423 | 8 | 85356084 | intron variant | A/G;T | snv | 1 | |||||
rs4826508 | X | 56785262 | intron variant | C/T | snv | 1 |