Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77010898 | 0.742 | 0.280 | 7 | 117642566 | stop gained | G/A;C | snv | 4.6E-04; 4.0E-06 | 13 | ||
rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 8 | |||
rs660652 | 1.000 | 0.080 | 15 | 78595490 | 3 prime UTR variant | A/G;T | snv | 3 | |||
rs886905373 | 0.925 | 0.120 | 14 | 94614481 | missense variant | G/A | snv | 2.8E-05 | 3 |