Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs711 | 0.851 | 0.200 | 21 | 38823135 | 3 prime UTR variant | A/C;G | snv | 4 | |||
rs461155 | 0.925 | 0.120 | 21 | 38819714 | synonymous variant | A/G;T | snv | 0.72; 4.0E-06 | 3 | ||
rs11254 | 0.925 | 0.120 | 21 | 38824464 | 3 prime UTR variant | C/T | snv | 0.34 | 2 | ||
rs2070531 | 0.925 | 0.120 | 21 | 38822292 | intron variant | C/T | snv | 0.35 | 2 | ||
rs11422952 | 21 | 38823618 | 3 prime UTR variant | TTTT/-;T;TTTTT;TTTTTT | delins | 1 |