Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs397514641 | 0.827 | 0.320 | 17 | 31169985 | stop gained | C/T | snv | 4.0E-06 | 1.4E-05 | 11 | |
rs137854550 | 0.790 | 0.360 | 17 | 31258500 | missense variant | A/C;G | snv | 10 | |||
rs587783031 | 0.851 | 0.120 | 5 | 112840255 | frameshift variant | A/-;AA | delins | 7 | |||
rs786202112 | 0.827 | 0.280 | 17 | 31327839 | missense variant | G/A | snv | 7 | |||
rs866445127 | 0.851 | 0.240 | 17 | 31352348 | stop gained | C/T | snv | 7 | |||
rs1057518842 | 1.000 | 0.080 | 17 | 31227215 | splice region variant | T/G | snv | 5 | |||
rs1057518904 | 0.882 | 0.240 | 17 | 31221932 | missense variant | A/G | snv | 5 | |||
rs1555534929 | 1.000 | 0.080 | 17 | 31337882 | splice donor variant | T/- | del | 4 | |||
rs267606600 | 1.000 | 0.120 | 17 | 31219018 | frameshift variant | AG/- | del | 1.4E-05 | 4 | ||
rs797045139 | 0.882 | 0.120 | 17 | 31327718 | missense variant | C/A;G;T | snv | 4 | |||
rs397514640 | 0.882 | 0.160 | 11 | 31802733 | missense variant | G/A | snv | 4 | |||
rs1555533285 | 1.000 | 0.080 | 17 | 31325859 | stop gained | C/G | snv | 3 | |||
rs1555618516 | 0.925 | 0.080 | 17 | 31258405 | missense variant | G/C | snv | 3 | |||
rs1555619056 | 0.925 | 0.160 | 17 | 31261858 | splice donor variant | G/A;C | snv | 3 |