Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1143627 | 0.605 | 0.760 | 2 | 112836810 | 5 prime UTR variant | G/A | snv | 0.56 | 47 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
rs1800875 | 0.742 | 0.360 | 14 | 24510132 | upstream gene variant | C/T | snv | 0.41 | 12 | ||
rs1324519932 | 0.925 | 0.160 | X | 30308445 | stop gained | C/A;G | snv | 1.3E-05 | 9.5E-06 | 2 | |
rs1555973010 | 0.925 | 0.160 | X | 30308463 | stop gained | G/A | snv | 2 | |||
rs1131691564 | 0.925 | 0.160 | X | 30308656 | stop gained | C/T | snv | 2 | |||
rs1555973115 | 0.925 | 0.160 | X | 30308812 | frameshift variant | TT/-;T | delins | 2 | |||
rs767828388 | 0.925 | 0.160 | X | 30308836 | stop gained | G/A;C | snv | 6.1E-06 | 2 | ||
rs1555973131 | 0.925 | 0.160 | X | 30308848 | stop gained | C/T | snv | 2 | |||
rs3132468 | 0.827 | 0.240 | 6 | 31507709 | intron variant | C/T | snv | 0.77 | 5 | ||
rs3740360 | 0.827 | 0.240 | 10 | 94265734 | intron variant | A/C | snv | 9.7E-02 | 8.4E-02 | 7 | |
rs3765524 | 0.724 | 0.320 | 10 | 94298541 | missense variant | C/T | snv | 0.27 | 0.31 | 17 |